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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 98951

34 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
April 27, 2026
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Medline Industries, LP

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

34 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 34

Medline EBSI Kit EBSI1534

Z-2414-2026
Recall number
Z-2414-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

UDI-DI 10653160350507 Lot 2025110490

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 2 of 34

Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716

Z-2415-2026
Recall number
Z-2415-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJRA2742 UDI-DI 10198459627330 Lot 26AMA185 DYNJRA2716 UDI-DI 10198459567988 Lot 25KBA971

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 3 of 34

BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A

Z-2416-2026
Recall number
Z-2416-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJRA2119A UDI-DI 10198459194702 lot 25LBB738 DYNJRA1011A UDI-DI 10888277783614 lots 25KBB849 25LBB734

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 4 of 34

MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G

Z-2417-2026
Recall number
Z-2417-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ84775A UDI-DI 10195327606527 lot 25LMH070 DYNJ47269D UDI-DI 10195327674786 lot 25LMJ234 DYNJ63276G UDI-DI 10198459458835 lot 26BBC598

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 5 of 34

Medline convenience kits: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y PACEMAKER DYNJ56297C PACEMAKER PK DYNJT3454 PACEMAKER/ICD PACK DYNJ33822L PAD OPEN HEART DYNJ900962O PEDIATRIC OPEN HEART DYNJ54238L DYNJT6766 STAZ BASIC VASCULAR DYNJ909794C VASCULAR ACCESS KIT CVI5323A VASCULAR CDS CDS983040M

Z-2418-2026
Recall number
Z-2418-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ61460C UDI-DI 10198459422133 lot 25KBA098 CDS840150Y UDI-DI 10198459303029 lots 25JBW220 26BBD028 DYNJ56297C UDI-DI 10198459513954 lot 25LMJ874 DYNJT3454 UDI-DI 10198459325663 lot 25KBG761 DYNJ33822L UDI-DI 10198459385582 lot 26AMA072 DYNJ900962O UDI-DI 10198459452581 lot 26CBC302 DYNJ54238L UDI-DI 10198459443114 lot 25LMH549 DYNJT6766 UDI-DI 10198459580888 lot 25KBM870 DYNJ909794C UDI-DI 10198459528002 lot 25LBF702 CVI5323A UDI-DI 10198459582035 lot 25KBM758 CDS983040M UDI-DI 10198459579813 lots 25KBO682 26BBB926

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 6 of 34

Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT A CATH CDS982047S VEIN ABLATION PACK DYNJ62889C

Z-2419-2026
Recall number
Z-2419-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNDC3525 UDI-DI 10198459576294 Lot 25KBM985 DT13191A UDI-DI 10653160998914 Lot 26AMA168 CDS982047S UDI-DI 10198459385735 Lot 26AMB202 DYNJ62889C UDI-DI 10198459416453 Lot 26AMA584

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 7 of 34

Medline convenience kits: BREAST-HERNIA-PORT CDS-LF CDS984853L

Z-2420-2026
Recall number
Z-2420-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

UDI-DI 10198459293535 Lots 26AME511 26AMG737

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 8 of 34

Medline convenience kits: DISCECTOMY PACK DYNJ86476B EAR DYNJ81460C DYNJ900004J DYNJ901779J DYNJ902900F EAR PACK DYNJ81419D ENT PACK DYNJ40498B HEAD & NECK CDS DYNJ901246J JEWISH DR SEVERTSON EAR DYNJ909252C JEWISH HEAD&NECK DYNJ909255C KIT HEAD AND NECK MHS DYNJ905364B MAJOR EAR CDS983347S MAJOR EAR FMOL LADY OF THE LAK DYNJ89581 MAJOR EAR PACK DYNJT4872 MAJOR HEAD AND NECK PACK DYNJ38985G MAJOR HEAD NECK PACK DYNJ45706B MZ EAR CDS DYNJ905642F PARATHYROID PACK DYNJ81389F PK,ENT-EAR DYNJ43700B SM-HEAD AND NECK PACK-LF DYNJ0780036W THYROID CDS CDS983693I TYMPANOPLASTY CDS982720S TYMPANOPLASTY MASTOIDECTOM DYNJ66231B TYMPANOPLASTY PACK-LF DYNJ62820D WH FACIAL HEAD AND NECK PACK DYNJ89028A WMC COCHLEAR IMPLANT ADD ON DYNJ907206G

Z-2421-2026
Recall number
Z-2421-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ86476B UDI-DI 10198459440366 Lot 25KBL478 DYNJ81460C UDI-DI 10198459434679 Lot 25KBE552 DYNJ900004J UDI-DI 10198459560354 Lot 26AMA112 DYNJ901779J UDI-DI 10193489979749 Lot 25LMI890 DYNJ902900F UDI-DI 10198459496936 Lot 25KBA607 DYNJ81419D UDI-DI 10198459113444 Lot 25KBM670 DYNJ40498B UDI-DI 10193489806779 Lots 25KBC776 25LBO494 DYNJ901246J UDI-DI 10198459447310 Lots 25KBQ989 26ABI798 26DBH373 DYNJ909252C UDI-DI 10198459318726 Lots 25JBS227 25KBC598 25LBR040 DYNJ909255C UDI-DI 10198459210167 Lot 25LBH411 DYNJ905364B UDI-DI 10198459346255 Lots 25LBM363 26BBO336 CDS983347S UDI-DI 10198459397370 Lots 26BBC029 26CBR342 DYNJ89581 UDI-DI 10198459278594 Lot 25LBP819 DYNJT4872 UDI-DI 10198459459672 Lot 25KBA908 DYNJ38985G UDI-DI 10195327385682 Lots 25JBA164 25KBG575 DYNJ45706B UDI-DI 10193489856293 Lot 25KBK200 DYNJ905642F UDI-DI 10195327587277 Lot 26AME607 DYNJ81389F UDI-DI 10198459394775 Lot 26BBC753 DYNJ43700B UDI-DI 10195327523039 Lot 25LBD750 DYNJ0780036W UDI-DI 10198459036972 Lot 25LMJ600 CDS983693I UDI-DI 10193489953848 Lot 25KBQ399 CDS982720S UDI-DI 10198459530258 Lots 25KBU081 25LBT481 26ABC446 DYNJ66231B UDI-DI 10195327341640 Lots 25JBY408 25KBK197 DYNJ62820D UDI-DI 10198459105463 Lot 25LMH554 DYNJ89028A UDI-DI 10198459472565 Lot 25KBI158 DYNJ907206G UDI-DI 10198459368028 Lot 25LBM564

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 9 of 34

Medline convenience kits: ABD PACK DYNJ81673B BARIATRIC DYNJ902515K BARIATRIC + DYNJ904119O BARIATRIC CDS CDS983883J BWNBORO LAP CHOLE PACK-LF DYNJ32836B CCSB KARIN JWIRE LUMPECTOMY DYNJ910459B CHRISTUS CHILDRENS LAP CHOLE DYNJ61165G CUH MINOR PACK-LF DYNJ60095B FREE FLAP CUSTOM PACK B DYNJ82736B FREE NIPPLE GRAFT DYNJ911160B GEN MINOR DYNJ900906L GEN SURG LAPAROSCOPY PACK DYNJ55248F GEN SURG MINOR PACK DYNJ69142F GENERAL LAP DYNJ61475A DYNJT3759 GENERAL LAP PACK DYNJ61515I DYNJT4452 GENERAL LAP PACK-LF DYNJ37208D GENERAL LAPAROSCOPY DYNJ905870G GENERAL LAPAROSCOPY PACK DYNJ17443T DYNJ45263B DYNJT4504 LAP CHOLE DYNJ45664D DYNJ912005 LAP CHOLE PACK DYNJ81695B LAP CHOLE PACK-LF DYNJ0614113C DYNJ0618369V LAP CHOLE PROCEDURE-LF CDS981184D LAP CHOLE RFD DYNJ906302F LAP CHOLE SURGICOUNT DYNJ45531G LAP CHOLE TOTE DYNJ908339F LAP GASTRIC BYPASS CDS CDS860146M LAP GASTRIC PACK DYNJ62065A LAP HERNIA RFD DYNJ906301F LAP PACK DYNJ38871J DYNJ51389A LAPAROSCOPIC CDS920082AC LAPAROSCOPIC PACK DYNJ52605K LAPAROSCOPIC PACK-LF PHS41736G LAPAROSCOPY PACK DYNJT8313 LAPAROSCOPY PACK-LF DYNJ02309D DYNJ0551175T LAPAROSCOPY UM RF DYNJ902324D LAPAROSCOPY-LF DYNJ903241B LAPAROTOMY PACK-LF DYNJ21091O LARGE ABDOMINAL PACK-LF PHS41737D LEX GENERAL LAPAROSCOPY DYNJ900969K MINOR GENERAL PACK DYNJT3884 MINOR PACK-LF DYNJ0105608I MINOR PK DYNJ61335D MINOR PROCEDURE CDS CDS981793G PEDIATRIC MOSES DYNJ58864B PK, GEN-LAPAROSCOPY DYNJ53837B RMC GENERAL LAPAROSCOPIC DYNJ907087C ROBOTIC GENERAL DYNJ906861D SM-GENERAL LAP PACK-LF DYNJ0780078W SMJ GENERAL ABDOMINAL PACK-LF DYNJ25765Q UOFL HOSP GENERAL LAPAROSCOPY DYNJ909321A

Z-2422-2026
Recall number
Z-2422-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ81673B UDI-DI 10195327494728 Lot 26AMA776 DYNJ902515K UDI-DI 10195327662608 Lot 25KBO749 DYNJ904119O UDI-DI 10198459073151 Lots 26ABB899 26ABI225 26ABJ235 CDS983883J UDI-DI 10198459429798 Lot 25KBK403 DYNJ32836B UDI-DI 10195327037369 Lot 25LMF151 DYNJ910459B UDI-DI 10198459477409 Lot 26AML096 DYNJ61165G UDI-DI 10198459386701 Lots 25LBO683 26ABE316 DYNJ60095B UDI-DI 10198459413377 Lots 25KBB960 25LBO686 DYNJ82736B UDI-DI 10198459038907 Lot 25LMG794 DYNJ911160B UDI-DI 10198459398001 Lot 26AMB749 DYNJ900906L UDI-DI 10198459408526 Lot 26AMG179 DYNJ55248F UDI-DI 10195327633486 Lot 25KBA350 DYNJ69142F UDI-DI 10198459478499 Lot 25LMF407 DYNJ61475A UDI-DI 10195327605797 Lot 25JBT649 DYNJT3759 UDI-DI 10198459351037 Lot 25KBJ720 DYNJ61515I UDI-DI 10198459542992 Lot 25KBI633 DYNJT4452 UDI-DI 10198459460678 Lot 25JBR785 DYNJ37208D UDI-DI 10195327434182 Lot 25LBJ032 DYNJ905870G UDI-DI 10198459394591 Lots 25JBP623 25LBR135 DYNJ17443T UDI-DI 10195327692971 Lot 25KBJ329 DYNJ45263B UDI-DI 10193489852394 Lot 25KBH088 DYNJT4504 UDI-DI 10198459456701 Lot 25LMI354 DYNJ45664D UDI-DI 10193489898514 Lot 25KBB002 DYNJ912005 UDI-DI 10198459597121 Lot 25KBT433 DYNJ81695B UDI-DI 10198459023453 Lot 25LMJ938 DYNJ0614113C UDI-DI 10198459352539 Lot 25KBC852 DYNJ0618369V UDI-DI 10889942826599 Lot 26BBC627 CDS981184D UDI-DI 10193489324815 Lot 26AMG257 DYNJ906302F UDI-DI 10198459419850 Lot 25KBG656 DYNJ45531G UDI-DI 10195327006037 Lots 25JBR413 25LBN719 26BBD403 DYNJ908339F UDI-DI 10198459409554 Lot 25KBM957 CDS860146M UDI-DI 10195327224547 Lots 25KBK359 26ABG747 26ABQ780 DYNJ62065A UDI-DI 10193489273472 Lot 25LMH990 DYNJ906301F UDI-DI 10198459419843 Lot 25LBA148 DYNJ38871J UDI-DI 10198459240218 Lot 25LMJ264 DYNJ51389A UDI-DI 10889942881222 Lot 25LBR750 CDS920082AC UDI-DI 10198459237324 Lot 25KBR576 DYNJ52605K UDI-DI 10198459254789 Lot 25LMG367 PHS41736G UDI-DI 10198459438745 Lot 25LMG005 DYNJT8313 UDI-DI 10198459697159 Lot 26CBD042 DYNJ02309D UDI-DI 10198459134432 Lot 25LBP128 DYNJ0551175T UDI-DI 10198459533419 Lot 25KBE001 DYNJ902324D UDI-DI 10198459125683 Lot 25KBQ907 DYNJ903241B UDI-DI 10193489818987 Lot 26ABF331 DYNJ21091O UDI-DI 10198459485183 Lots 25KBA313 26CBD177 PHS41737D UDI-DI 10198459438752 Lot 25LMG512 DYNJ900969K UDI-DI 10198459452314 Lot 26ABG612 DYNJT3884 UDI-DI 10198459366840 Lot 25JBX326 DYNJ0105608I UDI-DI 10198459533259 Lots 25KBA344 25KBM306 25LBE190 DYNJ61335D UDI-DI 10195327128586 Lot 25KBA763 CDS981793G UDI-DI 10198459493683 Lot 25KBT360 DYNJ58864B UDI-DI 10198459346965 Lot 25LBP018 DYNJ53837B UDI-DI 10193489209730 Lot 25LBP490 DYNJ907087C UDI-DI 10198459201301 Lot 26AMA102 DYNJ906861D UDI-DI 10198459293702 Lot 26AMC100 DYNJ0780078W UDI-DI 10195327633929 Lots 25JME845 25LMK134 DYNJ25765Q UDI-DI 10198459603679 Lot 25LMG846 DYNJ909321A UDI-DI 10195327545628 Lot 25KBT731

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 10 of 34

Medline convenience kits: BREAST IMAGING DYNJT5893 CHOG PLASTICS SYNJ10306A ENDO BREAST AUGMENTATION PACK DYNJ68023 FACIAL PLASTIC DYNJ909926C JVL - MODULE PLASTIC PK DYNJ84081B KIT MAJOR PLASTICS MOSES DYNJ905362C MEM MAXILLOFACIAL PACK-LF DYNJ0660040R MINOR BREAST PACK DYNJ89023A PLASTIC MAJOR SURGERY DYNJ902510M PLASTIC PACK DYNJ84766 PLASTIC PACK-LF DYNJ0578842M PLASTICS EXTREMITY PACK DYNJ63803C PLASTICS PK - NO SYR DYNJ62433D RR-ASC-RHINOPLASTY PACK-LF DYNJ81772C TRANSGENDER PACK DYNJT7588 WH PLASTIC MAJOR PACK DYNJ89048A

Z-2423-2026
Recall number
Z-2423-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJT5893 UDI-DI 10198459517839 Lot 25KBA123 SYNJ10306A UDI-DI 10193489296891 Lots 25LBO305 26CBD081 DYNJ68023 UDI-DI 10193489468083 Lot 25KBI169 DYNJ909926C UDI-DI 10198459423109 Lots 25LBC067 25LBR659 DYNJ84081B UDI-DI 10198459462474 Lot 25LMI881 DYNJ905362C UDI-DI 10198459346842 Lots 25KBN239 25LBF694 DYNJ0660040R UDI-DI 10889942220083 Lots 25JME572 26AMA936 DYNJ89023A UDI-DI 10198459388316 Lot 25KBC500 DYNJ902510M UDI-DI 10198459683374 Lots 26CBM279 26CBO942 DYNJ84766 UDI-DI 10195327414108 Lot 26BBC049 DYNJ0578842M UDI-DI 10193489288292 Lot 25LMG027 DYNJ63803C UDI-DI 10198459149825 Lots 25LBN476 26CBC156 DYNJ62433D UDI-DI 10198459498176 Lots 25KBC752 25KBM917 DYNJ81772C UDI-DI 10198459349362 Lots 25LMH594 25LMI396 DYNJT7588 UDI-DI 10198459635182 Lot 26AMA250 DYNJ89048A UDI-DI 10198459388477 Lot 26BBD124

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 11 of 34

Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB GENERAL LAPAROSCOPY PA DYNJ58305 CHRISTUS CH PEDIATRIC BASIC DYNJ61167G CVC INSERTION BUNDLE CVI3940A DAVINCI PACK SURGICOUNT DYNJ45544F EPCH BASIC PACK DYNJ83094C GENERAL PACK DYNJ39682B DYNJ84882 GENERAL RFD DYNJ906336F GENERAL SURGERY PACK DYNJT6003 GV MACD PACK DYNJ46952M IMPLANT PACK - BBI AR DYNJ63508A KIT THORACOSCOPY DYNJ908872F LVAD TRAY DM1120A MAJOR UROLOGY PACK-LF DYNJ0368525M MICRODISECT DECOMPRESS-LF DYNJ911467 MINOR PACK DYNJ86972 MULTI PURPOSE PACK DYNJ58406B OPEN HEART DYNJ903245C P&K PACK DYNJT5838 PACK,PEDIATRIC MAJOR DYNJ906888F PCNL DYNJ904468C PEDIATRIC MINOR RFD DYNJ906296I PEDIATRIC PACK DYNJ54239K PEDIATRIC SURGERY DYNJ81474B PERLMUTTER PACK DYNJT7387 RFT ISC NOBLES MINOR PACK DYNJ43954B ROBOTICS FMOL LADY OF THE LAKE DYNJ89584 ROBOTICS PACK DYNJ83622B SCOLI PACK NTX DYNJ68415C SMALL ABDOMINAL PACK-LF PHS41749G STIM IMPLANT TRIALS DYNJ87790A SUPPLEMENTAL PACK DYNJ65244 TENEX PACK DYNDH2190 THORACIC PACK DYNJ56616G THORACIC PACK SHD DYNJ68416C THORACOSCOPY DYNJ9425843R THORACOTOMY PM DYNJ906815A THORACOTOMY THORACOSCOPY DYNJ902882D TRAY,NEONATAL PICC DRSG CHANGE DYNDC1533B UNIVERSAL-ASC DYNJ900071C

Z-2424-2026
Recall number
Z-2424-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ905869G UDI-DI 10198459394577 Lot 25JBX559 DYNJ68484B UDI-DI 10198459368967 Lot 25LME889 DYNJ58305 UDI-DI 10889942843763 Lot 25KBA708 DYNJ61167G UDI-DI 10198459386671 Lots 25KBN904 25LBQ928 CVI3940A UDI-DI 10653160998976 Lot 26AME675 DYNJ45544F UDI-DI 10193489876130 Lot 25KBJ042 DYNJ83094C UDI-DI 10198459562051 Lot 25JMD330 DYNJ39682B UDI-DI 10193489769241 Lots 25KBI410 25LBI978 26BBC735 DYNJ84882 UDI-DI 10195327432324 Lot 26CBQ487 DYNJ906336F UDI-DI 10198459419959 Lots 25KBR497 26CBO946 DYNJT6003 UDI-DI 10198459531255 Lots 25JBV850 26CBC211 DYNJ46952M UDI-DI 10198459090134 Lots 25KBH401 25LBO238 DYNJ63508A UDI-DI 10193489363845 Lot 26BBC181 DYNJ908872F UDI-DI 10198459660306 Lot 26BBR620 DM1120A UDI-DI 10653160998891 Lots 25KBA425 25LBJ075 DYNJ0368525M UDI-DI 10193489820249 Lots 25KBG895 25KBG896 DYNJ911467 UDI-DI 10198459358562 Lot 25LBA393 DYNJ86972 UDI-DI 10195327694296 Lot 26CBD230 DYNJ58406B UDI-DI 10193489957228 Lot 25JBT217 DYNJ903245C UDI-DI 10889942890170 Lot 26ABG614 DYNJT5838 UDI-DI 10198459513329 Lot 25JBT808 DYNJ906888F UDI-DI 10198459194764 Lot 26AMC879 DYNJ904468C UDI-DI 10195327631413 Lot 25KBL838 DYNJ906296I UDI-DI 10198459419829 Lot 25KBN303 DYNJ54239K UDI-DI 10198459443206 Lot 25LMG373 DYNJ81474B UDI-DI 10198459100260 Lot 25JBY253 DYNJT7387 UDI-DI 10198459615924 Lot 26CBQ932 DYNJ43954B UDI-DI 10193489509168 Lot 25LMI928 DYNJ89584 UDI-DI 10198459278723 Lots 25JBS433 25LBO815 25LBP820 DYNJ83622B UDI-DI 10198459402739 Lots 25JBA251 25JBX613 DYNJ68415C UDI-DI 10195327341749 Lots 25KBM185 26BBD267 PHS41749G UDI-DI 10198459438844 Lot 25LMG971 DYNJ87790A UDI-DI 10198459358968 Lots 25KBC718 25KBC975 DYNJ65244 UDI-DI 10193489257434 Lots 25KBC479 26CBC173 DYNDH2190 UDI-DI 10198459467967 Lots 25KBE086 25KBM732 DYNJ56616G UDI-DI 10198459533167 Lots 25LBD705 26CBC585 DYNJ68416C UDI-DI 10195327341688 Lot 25KBH744 DYNJ9425843R UDI-DI 10198459085499 Lot 25KMC242 DYNJ906815A UDI-DI 10195327027018 Lot 26BBO802 DYNJ902882D UDI-DI 10198459496790 Lot 25LBR117 DYNDC1533B UDI-DI 10889942813926 Lot 25JBU460 DYNJ900071C UDI-DI 10198459121722 Lots 26AMH365 26AMH758

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 12 of 34

Medline convenience kit: IV START KIT W/HUBGUARD DYNDV2662

Z-2425-2026
Recall number
Z-2425-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

UDI-DI 10653160378518 Lot 26CBC731

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 13 of 34

Medline convenience kit: KIT: DRESSING CHANGE PED DYNDC3359

Z-2426-2026
Recall number
Z-2426-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

UDI-DI 10195327495589 Lots 25KBK310 25LBN341

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 14 of 34

Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D

Z-2427-2026
Recall number
Z-2427-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

UDI-DI 10198459409431 Lot 25KBB755

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 15 of 34

Medline convenience kit: BHS NEURO DYNJ904900N MEDTRX NEURO PACK DYNJ67267B MRI DBS PACK DYNJ9814630O NEURO CDS-LF CDS983383L NEURO PACK DYNJ59397Q DYNJT7315 NEURO PACK-LF DYNJ25097I NEURO VP SHUNT/VAGAL NERVE-RF DYNJ21925S PK NEURO SHUNT BUMC DYNJT6428 RR-NEURO DBS HEAD PACK-LF DYNJ0785736M VP SHUNT SYNJ10307B

Z-2428-2026
Recall number
Z-2428-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ904900N UDI-DI 10198459504273 Lot 25LBB457 DYNJ67267B UDI-DI 10198459084331 Lot 25LBQ732 DYNJ9814630O UDI-DI 10195327587291 Lot 25LBD665 CDS983383L UDI-DI 10198459224577 Lot 25LBC092 DYNJ59397Q UDI-DI 10198459495427 Lot 25LMG049 DYNJT7315 UDI-DI 10198459620225 Lot 25LBO095 DYNJ25097I UDI-DI 10198459449550 Lot 25KBC747 DYNJ21925S UDI-DI 10195327105020 Lots 25KBD835 25LBR371 DYNJT6428 UDI-DI 10198459553660 Lot 26AMA602 DYNJ0785736M UDI-DI 10198459487149 Lot 25LMI831 SYNJ10307B UDI-DI 10195327007249 Lot 25LBE309

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 16 of 34

Medline convenience kit: (82)LABOR & DELIVERY C-SECTION DYNJ907895F

Z-2429-2026
Recall number
Z-2429-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

UDI-DI 10198459366390 Lot 25KBL873

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 17 of 34

Medline convenience kit: SMSC-PELVISCOPY PACK-LF DYNJ0161619M

Z-2430-2026
Recall number
Z-2430-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

UDI-DI 10198459028274 Lot 25LMI820

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 18 of 34

Medline convenience kits: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I GENERAL ROBOTICS PACK DYNJT8308 GYN LAP CDS860087Q GYN LAPAROSCOPY DYNJ910084C GYN LAPAROSCOPY CDS CDS982371I GYN LAPAROSCOPY CDS #34-RF CDS920099S GYN LAPAROSCOPY PACK DYNJT3887 DYNJT6876 GYN ROBOTIC CDS CDS984228K GYN ROBOTICS DYNJ911843 KIT LABOR DELIVERY TUBAL LIGAT DYKMBNDL165C ROBOTIC LAP CHOLE CDS CDS985442J ROBOTIC PACK DYNJ84725B DYNJ910594B ROBOTIC SURGERY PACK DYNJ53711B ROBOTICS PACK DYNJ83622C UOFL GYN LAPAROSCOPY DYNJ909322B WMC ROBOTIC PACK - LF DYNJ902583O

Z-2431-2026
Recall number
Z-2431-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ905836D UDI-DI 10195327517977 Lot 25LBB534 DYNJ905293I UDI-DI 10198459247972 Lot 25KBM585 DYNJT8308 UDI-DI 10198459697135 Lot 26CBD040 CDS860087Q UDI-DI 10198459543005 Lots 25JBV094 25LBP061 DYNJ910084C UDI-DI 10198459597466 Lot 25LBE810 CDS982371I UDI-DI 10198459044106 Lots 25KBH343 26CBN241 CDS920099S UDI-DI 10195327140656 Lot 25KBO172 DYNJT3887 UDI-DI 10198459366871 Lot 25JBX564 DYNJT6876 UDI-DI 10198459583148 Lot 25KBM646 CDS984228K UDI-DI 10198459044113 Lot 26ABF608 DYNJ911843 UDI-DI 10198459555206 Lot 25LBC203 DYKMBNDL165C UDI-DI 10198459634284 Lot 25LBR024 CDS985442J UDI-DI 10198459476686 Lot 25JBT926 DYNJ84725B UDI-DI 10198459366949 Lot 25JBA329 DYNJ910594B UDI-DI 10198459563768 Lot 25KBJ104 DYNJ53711B UDI-DI 10198459023538 Lots 25KBF929 25LBB875 DYNJ83622C UDI-DI 10198459607172 Lots 25LBR740 26CBJ460 DYNJ909322B UDI-DI 10198459443848 Lot 25LBD961 DYNJ902583O UDI-DI 10198459441806 Lot 25LBC041

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 19 of 34

Medline convenience kits: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ69533C

Z-2432-2026
Recall number
Z-2432-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ904305J UDI-DI 10198459268151 lot 25KBT972 DYNJ69533C UDI-DI 10198459524097 lot 26BBC483

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 20 of 34

Medline convenience kits: WT LAVH PACK DYNJ46609F

Z-2433-2026
Recall number
Z-2433-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ46609F UDI-DI 10198459403989 lot 25JBS436

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 21 of 34

Medline convenience kits: DAVINCI MAIN DYNJ908031D

Z-2434-2026
Recall number
Z-2434-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ908031D UDI-DI 10198459632297 lot 26AMB067

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 22 of 34

Medline convenience kits: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS760053K

Z-2435-2026
Recall number
Z-2435-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ905154I UDI-DI 10198459549977 lots 26ABB308 26BBA671 CDS760053K UDI-DI 10195327182977 lot 25KBP010

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 23 of 34

Medline convenience kits: ACD DYNJ904999J ACDF DYNJ907336B DYNJ910821A ACDF PACK DYNJ81098C ACL DYNJ911996 ACL ACCESSORY PACK DYNJ86584B ACL- LF DYNJ905281B ACL PACK DYNJ67271A ALIF DYNJ904848L ANTERIOR CERVICAL DYNJ901355J ARTHROSCOPY DYNJ908193B ARTHROSCOPY PACK-LF DYNJ42963M DYNJ52268B ARTHROSCOPY SHOULDER DYNJ908684A BACK CDS-LF CDS983364G BACK PACK DYNJT4339 CDH SPINE PACK DYNJ908828D CERVICAL CDS DYNJ903477J CMC ORTHO BACK TRAY SYNJ10272B CRANIOTOMY DYNJ911853 CRANIOTOMY ROOSEVELT PACK DYNJ58358F CUSTOM HAND PACK-LF DYNJ0537135V CUSTOM SPINAL PACK DYNJT7544 DISCECTOMY PACK DYNJ86770 DJ ORTHO SPINE DYNJ48980M EXTREMITY PACK-LF DYNJT4161 FOOT PACK DYNJ53179D GENERAL ORTHO-ACNW DYNJ84891 GILMORE SHOULDER SCOPE PACK DYNJ58002 GV LUMBAR LAMINECTOMY PK DYNJ46938L HAND PACK DYNJ63113B DYNJ69662A DYNJT5855 HAND-LF DYNJ903263B KIT LAMINECTOMY DYNJ908806C KNEE ARTHROSCOPY DYNJ902056C DYNJ904846I KNEE ARTHROSCOPY-LF DYNJ905871F KNEE SCOPE DYNJ906986G LAMINECTOMY DYNJ904847K DYNJ909505D LAMINECTOMY CDS CDS983115K LAMINECTOMY CERVICAL DISC-LF DYNJ905286G LAMINECTOMY NEURO PACK DYNJ58356F LAMINECTOMY SPINE DYNJ904139L LOWER EXTREMITY PACK DYNJ63114C LUMBAR CERVICAL PACK-LF DYNJ0101088G LUMBAR LAMI DYNJ905020J LUMBAR LAMINECTOMY DYNJ53707 LUMBAR LAMINECTOMY PACK DYNJT4386 MAIN/LAMINECTOMY PACK-LF DYNJ0565499AN NJ SPINE SPECIALIST PACK DYNJ58706F OHOW SPINE-BACK PACK DYNJ910097A ORTHO NECK CDS-LF CDS983134C ORTHO PACK-LF DYNJ37202G ORTHO SPINE DYNJ40221G OSC BEACH CHAIR SHOULDER-LF DYNJ905282C PACC PETRIE ACL ADD ON PACK-LF DYNJ58290D PACK,ARTHROSCOPY ASC DYNJ65484A PACK,POSTERIOR SPINAL FUSION DYNJ906892B PAD LATERAL SPINE DYNJ902158L DYNJ902158M PAD POSTERIOR SPINE DYNJ902142L PK-SPINE DYNJ58259A PODIATRY PACK DYNJ62288D POST SPINE PACK DYNJ20509R POSTERIOR SPINAL FUSION DYNJ903250B RFT ARTHROSCOPY PACK DYNJ43956C RFT SHOULDER PACK-NOBLE DYNJ36331D SA SHOULDER #2 BORDEN DYNJ56501A SHOULDER DYNJ900893M DYNJ904184I SHOULDER ARTHROSCOPY DYNJ904842G SHOULDER PACK DYNJ83483 SHOULDER PACK-LF DYNJ42973N SHOULDER SCOPE PACK NTX DYNJ68399C SPINAL PACK DYNJ49692G SPINE DYNJ910451A SPINE PACK DYNJ20147O DYNJ84971 DYNJ86044A DYNJ86308C DYNJ88917 DYNJS3069 DYNJT4163 DYNJT8396 ST CHARLES TOTAL HIP DYNJ909593C TOTAL HIP DYNJ910906D TOTAL HIP PACK DYNJ64156B TOTAL JOINT DYNJ904186G TOTAL KNEE PACK DYNJ60967 DYNJ61409A WMC ORTHO SPINE WMC-LF DYNJ902528M XLIF DYNJ910795B

Z-2436-2026
Recall number
Z-2436-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ904999J UDI-DI 10195327305024 lot 26DBJ301 DYNJ907336B UDI-DI 10198459084300 lot 26DBF966 DYNJ910821A UDI-DI 10198459453359 lots 25KBH623 26BBL877 26BBM089 DYNJ81098C UDI-DI 10198459357107 lots 25JBR783 25KBD860 DYNJ911996 UDI-DI 10198459596230 lots 25LBI311 25LBV123 26ABN955 DYNJ86584B UDI-DI 10198459410604 lot 25LMH561 DYNJ905281B UDI-DI 10195327063191 lot 25KBD109 DYNJ67271A UDI-DI 10195327626822 lot 25JBV609 DYNJ904848L UDI-DI 10198459217500 lot 26DBK390 DYNJ901355J UDI-DI 10198459224775 lot 25LBK865 DYNJ908193B UDI-DI 10198459521720 lot 25LBD958 DYNJ42963M UDI-DI 10198459611834 lot 26AMB027 DYNJ52268B UDI-DI 10195327432423 lots 25LBC027 26CBA143 DYNJ908684A UDI-DI 10198459500510 lot 26AMH337 CDS983364G UDI-DI 10195327432508 lot 26BBR233 DYNJT4339 UDI-DI 10198459448720 lot 26CBC179 DYNJ908828D UDI-DI 10198459512919 lots 25KMC466 26AMG065 DYNJ903477J UDI-DI 10195327565206 lots 26AMG182 26AMG272 SYNJ10272B UDI-DI 10195327006532 lot 25LBO306 DYNJ911853 UDI-DI 10198459559372 lot 25KBI658 DYNJ58358F UDI-DI 10198459105029 lots 25JBX146 25LBP519 DYNJ0537135V UDI-DI 10195327556389 lots 25KBG081 25LBP178 26BBC915 DYNJT7544 UDI-DI 10198459631399 lots 25LBN779 DYNJ86770 UDI-DI 10195327674229 lot 25KBJ623 DYNJ48980M UDI-DI 10195327533694 lot 25LMK166 DYNJT4161 UDI-DI 10198459410741 lot 25JBA211 DYNJ53179D UDI-DI 10198459574658 lot 25LMH296 DYNJ84891 UDI-DI 10195327434151 lot 25JBT703 DYNJ58002 UDI-DI 10889942807383 lot 25LBO695 DYNJ46938L UDI-DI 10198459090103 lot 25JBS479 DYNJ63113B UDI-DI 10195327131449 lot 25KBJ559 DYNJ69662A UDI-DI 10198459132360 lot 25JBX052 DYNJT5855 UDI-DI 10198459515057 lots 25JBV938 25LBO691 DYNJ903263B UDI-DI 10889942754014 lot 26CBQ083 DYNJ908806C UDI-DI 10198459285868 lot 25LMJ639 DYNJ902056C UDI-DI 10195327422103 lots 25JBU940 25LBR965 DYNJ904846I UDI-DI 10198459217579 lot 26CBS964 DYNJ905871F UDI-DI 10198459206252 lot 25LBA302 DYNJ906986G UDI-DI 10198459610226 lot 26AMJ169 DYNJ904847K UDI-DI 10198459217586 lot 25KBR022 DYNJ909505D UDI-DI 10198459594229 lot 25LMJ127 CDS983115K UDI-DI 10198459579608 lot 25LBE987 DYNJ905286G UDI-DI 10198459248184 lots 26AMA067 26AMH307 DYNJ58356F UDI-DI 10198459104923 lot 25LBR764 DYNJ904139L UDI-DI 10198459528583 lot 25JBT916 DYNJ63114C UDI-DI 10193489870206 lot 25JBX122 DYNJ0101088G UDI-DI 10198459619960 lot 25LBQ608 DYNJ905020J UDI-DI 10198459548314 lot 25KBJ908 DYNJ53707 UDI-DI 10889942441082 lots 25LBP985 26CBR371 DYNJT4386 UDI-DI 10198459457609 lot 25KBK189 DYNJ0565499AN UDI-DI 10195327318352 lot 25JMF339 DYNJ58706F UDI-DI 10198459124877 lot 26CBC852 DYNJ910097A UDI-DI 10198459504785 lot 26AMD592 CDS983134C UDI-DI 10195327147655 lot 25KBT474 DYNJ37202G UDI-DI 10195327685393 lots 25JBS464 25LBR525 DYNJ40221G UDI-DI 10198459448515 lot 25LMJ294 DYNJ905282C UDI-DI 10195327393069 lot 25KBM844 DYNJ58290D UDI-DI 10195327513467 lot 25LBQ039 DYNJ65484A UDI-DI 10195327303501 lot 25LMB980 DYNJ906892B UDI-DI 10198459168611 lots 25KBG661 26BBC906 DYNJ902158L UDI-DI 10198459453021 lot 25LBD928 DYNJ902158M UDI-DI 10198459681721 lot 26DBK385 DYNJ902142L UDI-DI 10198459452970 lot 25LBA949 DYNJ58259A UDI-DI 10193489734034 lots 25JBY406 25LBM865 DYNJ62288D UDI-DI 10195327605827 lots 25JBA294 25KBB258 DYNJ20509R UDI-DI 10198459277849 lots 25LMH654 26AMB105 DYNJ903250B UDI-DI 10889942755288 lot 25KBM855 DYNJ43956C UDI-DI 10193489970708 lot 25KBL821 DYNJ36331D UDI-DI 10198459416446 lot 25LMH136 DYNJ56501A UDI-DI 10195327310752 lot 25LMI162 DYNJ900893M UDI-DI 10198459408632 lots 25KMB298 26AMB284 DYNJ904184I UDI-DI 10198459640704 lot 26CBO500 DYNJ904842G UDI-DI 10198459217753 lot 25LBC835 DYNJ83483 UDI-DI 10195327268916 lot 25KBH325 DYNJ42973N UDI-DI 10198459621178 lot 26AMA642 DYNJ68399C UDI-DI 10195327341763 lot 26BBD183 DYNJ49692G UDI-DI 10195327347352 lot 26AMA587 DYNJ910451A UDI-DI 10198459365560 lot 25KBG700 26ABF330 DYNJ20147O UDI-DI 10198459377617 lot 25JBA158 DYNJ84971 UDI-DI 10195327442620 lot 26BBC185 DYNJ86044A UDI-DI 10198459404351 lot 25LBQ169 DYNJ86308C UDI-DI 10198459425233 lot 25LBQ110 DYNJ88917 UDI-DI 10198459215926 lot 25LMF333 DYNJS3069 UDI-DI 10888277058286 lot 25LBC215 DYNJT4163 UDI-DI 10198459410758 lot 26BBC139 DYNJT8396 UDI-DI 10198459704871 lot 26CBE087 DYNJ909593C UDI-DI 10198459523816 lot 25LBB787 DYNJ910906D UDI-DI 10198459472626 lot 25KBJ090 DYNJ64156B UDI-DI 10195327678746 lots 25KBC275 25LBC916 26CBC871 DYNJ904186G UDI-DI 10198459002922 lots 25KBG639 25LBB568 DYNJ60967 UDI-DI 10193489537918 lot 25LMJ893 DYNJ61409A UDI-DI 10193489778595 lots 25LMH863 26AMC051 DYNJ902528M UDI-DI 10198459445873 lot 25KBU092 DYNJ910795B UDI-DI 10198459594205 lot 25LMH707

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 24 of 34

Centurion convenience kits: CENTRAL LINE DRESSING SV43 FCP DYNDC2356B DIALYSIS CATHETER MAINTENANCE KIT DT17570 DIALYSIS DRESSING CHANGE KIT DT21370B DRESSING CHANGE TRAY - GOLD DT21115B PORT DRESSING CHANGE KIT DYNDC2815A

Z-2437-2026
Recall number
Z-2437-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNDC2356B UDI-DI 10653160327271 Lot 2025102090 DT17570 UDI-DI 10653160266891 Lot 2025102290 DT21370B UDI-DI 10653160360643 Lot 2025102290 DT21115B UDI-DI 10653160360681 Lot 2025111490 DYNDC2815A UDI-DI 10653160357070 Lot 2025110590

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 25 of 34

Medline convenience kits: CMH CENTRAL LINE DRESSING CHANGE KIT EBSI1705A CVC/PICC/MIDLINE DRESSING CHANGE KIT EBSI1057A DIALYSIS DRESSING CHANGE EBSI1498 EBSI CVC DRESSING CHANGE KIT EBSI1585 PICC DRESSING CHANGE TRAY EBSI1621 PORT ACCESS KIT EBSI1837

Z-2438-2026
Recall number
Z-2438-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

EBSI1705A UDI-DI 10653160382850 Lot 2025103090 EBSI1057A UDI-DI 10653160356875 Lot 2025120890 EBSI1498 UDI-DI 10193489111538 Lot 2025110690 EBSI1585 UDI-DI 10653160354796 Lot 2025102190 EBSI1621 UDI-DI 10653160358336 Lot 2025110390 EBSI1837 UDI-DI 10653160388555 Lot 2025102990

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 26 of 34

Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC INSERTION KIT ECVC8055A VANTEX PI CVC 7F, 3L, 20CM BUNDLE ECVC6915A ECVC6985B

Z-2439-2026
Recall number
Z-2439-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

ECVC6805B UDI-DI 10653160387428 Lot 2025120890 ECVC8055A UDI-DI 10653160387848 Lot 2025112690 ECVC6915A UDI-DI 10653160389439 Lot 2025102790 ECVC6985B UDI-DI 10653160388272 Lot 2025103190

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 27 of 34

Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING CHANGE KIT EBSI1328A

Z-2440-2026
Recall number
Z-2440-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

EBSI1688 UDI-DI 10653160370130 Lot 2025102890 EBSI1328A UDI-DI 10653160382980 Lot 2025103090

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 28 of 34

Medline convenience kits: ACL PACK DYNJ64161C ARTHROSCOPY PACK DYNJ47103D DYNJ67197G DYNJ85197A DYNJT4007 BASIC ACCESS PACK-LF DYNJ36698B BASIC BACK TRAY DYNJ89037 BASIC PEDI PACK-LF DYNJ0171446I DYNJ0171446J BASIC SPINE DYNJ910915A BREAST PACK DYNJ87587A BREAST PLASTIC PACK DYNJ84482C C SECTION DYNJ49172I CAROTID ENDARTERECTOMY PACK DYNJ48013L CENTRAL LINE PACK-LF DYNJ0220136S CERVICAL FUSION DYNJ908135B CERVICAL SPINE PACK DYNJ53044G C-SECTION DYNJ909099F DAVINCI PROSTATE PACK DYNJ61711C DEPAUL FOOT & ANKLE-LF DYNJ20010L DIEP PACK DYNJ64964J DYNJ43210K DYNJ61787F DYNJ87065 EAR CUSTOM PACK DYNJ82564A ENT FREE FLAP PACK SAFETY DYNJ54720D EP PACEMAKER SAFETY #1 DYNJ54722F EPCH EXTREMITY PACK DYNJ83095B EXTREMITY PACK DYNJ32934F EXTREMITY PACK-LF DYNJ68935B FISTULA PACK DYNJ66502B GENDER AFFIRMING SURGERY DYNJ66252F GYN LAPAROSCOPY PACK AHSC DYNJT8381 HAND PACK WATCHMAKER-LF DYNJ34580D HEAD & NECK PACK-LF DYNJ0282388T DYNJ88308 HIP SCOPE DYNJ907120D KNEE ARTHRO PACK DYNJ58404F KNEE ARTHROSCOPY PACK DYNJ84740A LAMI OVERHEAD PACK DYNJ46531Q LAMINECTOMY NEURO MPH DYNJT5271 LAMINECTOMY PACK DYNJ68785D LAP APPY PACK DYNJT6005 LAP CHOLE PACK DYNJ82087A LEVY PACK DYNJ83939C MAJOR LAP VCH DYNJ39217P MAJOR NEURO PACK-LF DYNJ0578916AA MAJOR PACK DYNJ58528J MINOR GEN PACK DYNJ61661B MINOR LAPAROTOMY PACK-LF DYNJ0753436P MINOR PACK DYNJ54968B NEURO PACK DYNJ67628D NEURO SHUNT PACK-LF DYNJ0578815W OMFS PACK DYNJ54400C OPEN HEART PACK DYNJT5008 OPEN HEART-LF DYNJ48260F OPEN LAPAROTOMY PACK DYNJ39247I DYNJ39247J PACEMAKER PACK DYNJ31461I DYNJ61411C PACK,ORTHO FLIP DYNJ65471B PED OPEN HEART PACK DYNJ45373G PLASTIC PACK DYNJ82495D PLASTICS PK - NO SYR DYNJ62433F PODIATRY PACK OP7809M PPE BUNDLE KIT DT13351A PROSTATE ROBOTIC PACK DYNJ84120C RADIAL ART LINE INSERTION ARTNC234 ROBOTIC GENERAL WHH DYNJT5376 ROBOTIC PACK DYNJ47978G RR-SPINE PACK DYNJ62643B SHOULDER ARTH PACK DYNJ58410D SHOULDER ARTHROSCOPY PACK DYNJ54477C DYNJT8391 SHOULDER PACK DYNJ61052B DYNJT3266 SHOULDER PACK-LF DYNJ0122428K PHS656414I SPINE PACK DYNJ64949C DYNJ83649B SPINE SHOULDER PACK DYNJ47104D STERILE ACCESS KIT DYNDA2664 TOTAL KNEE PACK DYNJ84741B TUBAL PACK DYNJ68253F UNIVERSAL PACK DYNJ83246B VA TAMPA GENERAL ROBOTIC PACK DYNJT6993 W.C. MINOR LAPAROTOMY PK-LF DYNJ0509186J ZALE OTOLOGY CDS CDS983181G

Z-2441-2026
Recall number
Z-2441-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ64161C UDI-DI 10198459146961 Lot 25KBH332 DYNJ47103D UDI-DI 10198459625008 Lot 25LMF684 DYNJ67197G UDI-DI 10198459481994 Lot 25JBA258 DYNJ85197A UDI-DI 10198459217395 Lot 25LMF727 DYNJT4007 UDI-DI 10198459381867 Lot 26BBC180 DYNJ36698B UDI-DI 10198459081811 Lots 25KBM204 26CBD413 DYNJ89037 UDI-DI 10198459229855 Lots 25KBI083 25KBM202 DYNJ0171446I UDI-DI 10195327589516 Lot 25JBT239 DYNJ0171446J UDI-DI 10198459591754 Lot 26CBB295 DYNJ910915A UDI-DI 10198459424960 Lot 25LBD596 DYNJ87587A UDI-DI 10198459114199 Lot 25JBR735 DYNJ84482C UDI-DI 10198459362491 Lot 26BBU043 DYNJ49172I UDI-DI 10198459042003 Lot 26AMA388 DYNJ48013L UDI-DI 10198459560941 Lot 25LBP624 DYNJ0220136S UDI-DI 10198459566073 Lot 25LMF648 DYNJ908135B UDI-DI 10198459586552 Lots 25LBC200 25LBR878 DYNJ53044G UDI-DI 10198459448768 Lot 25LMG369 DYNJ909099F UDI-DI 10198459375996 Lot 25JMF136 DYNJ61711C UDI-DI 10198459096754 Lot 25JBT124 DYNJ20010L UDI-DI 10198459229053 Lot 25JMD853 DYNJ64964J UDI-DI 10198459254109 Lot 25LMI867 DYNJ43210K UDI-DI 10198459546792 Lot 25LMI070 DYNJ61787F UDI-DI 10198459169694 Lot 25JBU635 DYNJ87065 UDI-DI 10198459007439 Lots 25KBD819 25LBP631 DYNJ82564A UDI-DI 10198459497551 Lot 25LBD560 DYNJ54720D UDI-DI 10195327549510 Lot 26CBC228 DYNJ54722F UDI-DI 10195327549633 Lots 25KBB967 25LBQ696 26CBE680 DYNJ83095B UDI-DI 10198459562068 Lot 25JMD325 DYNJ32934F UDI-DI 10195327697181 Lot 26CBC762 DYNJ68935B UDI-DI 10198459440373 Lot 25LBN254 DYNJ66502B UDI-DI 10198459395321 Lot 25KBC481 DYNJ66252F UDI-DI 10198459185397 Lot 25LBP873 DYNJT8381 UDI-DI 10198459702358 Lot 26CBD354 DYNJ34580D UDI-DI 10195327579661 Lot 25LMF989 DYNJ0282388T UDI-DI 10198459591990 Lot 25LBP896 DYNJ88308 UDI-DI 10198459143328 Lot 25KBJ822 DYNJ907120D UDI-DI 10198459427985 Lots 25KBK051 25KBT376 26DBF975 DYNJ58404F UDI-DI 10198459366413 Lots 25KBI176 26CBE677 DYNJ84740A UDI-DI 10198459421556 Lot 25KBB657 DYNJ46531Q UDI-DI 10198459526107 Lot 25LMJ845 DYNJT5271 UDI-DI 10198459471452 Lot 25LBC165 DYNJ68785D UDI-DI 10198459546952 Lot 25JBU924 DYNJT6005 UDI-DI 10198459531187 Lot 25JBU086 DYNJ82087A UDI-DI 10198459078019 Lot 25LMH034 DYNJ83939C UDI-DI 10198459342523 Lot 25JBY263 DYNJ39217P UDI-DI 10198459102356 Lot 25JME213 DYNJ0578916AA UDI-DI 10198459117565 Lot 25JME873 DYNJ58528J UDI-DI 10198459322815 Lot 26CBE343 DYNJ61661B UDI-DI 10198459096785 Lot 25KBA722 DYNJ0753436P UDI-DI 10198459466854 Lot 25LMJ282 DYNJ54968B UDI-DI 10198459428753 Lot 25KBD827 DYNJ67628D UDI-DI 10198459383373 Lot 25LMG428 DYNJ0578815W UDI-DI 10198459466892 Lot 25LMI628 DYNJ54400C UDI-DI 10195327646905 Lot 25KBI070 DYNJT5008 UDI-DI 10198459463525 Lot 26BBC492 DYNJ48260F UDI-DI 10198459220241 Lot 25KBL822 DYNJ39247I UDI-DI 10195327633509 Lot 25JBR808 DYNJ39247J UDI-DI 10198459640698 Lot 26BBD397 DYNJ31461I UDI-DI 10198459519734 Lot 25JBV372 DYNJ61411C UDI-DI 10198459493591 Lot 25KBA043 DYNJ65471B UDI-DI 10198459168574 Lot 25JMF211 DYNJ45373G UDI-DI 10198459254635 Lot 25LMI203 DYNJ82495D UDI-DI 10198459439834 Lots 25KBI927 25LBR381 DYNJ62433F UDI-DI 10198459627514 Lot 25LBO801 OP7809M UDI-DI 10198459368493 Lot 26CBB615 DT13351A UDI-DI 10653160325581 Lots 25JBA293 25KBB632 DYNJ84120C UDI-DI 10198459574177 Lot 26AMA032 ARTNC234 UDI-DI 10198459566974 Lot 25KBJ985 DYNJT5376 UDI-DI 10198459470783 Lot 25LBP929 DYNJ47978G UDI-DI 10198459416606 Lot 26AMA586 DYNJ62643B UDI-DI 10198459164446 Lot 25LMG407 DYNJ58410D UDI-DI 10198459366468 Lot 25LBI975 DYNJ54477C UDI-DI 10198459004155 Lot 25LMI210 DYNJT8391 UDI-DI 10198459703140 Lot 26CBJ555 DYNJ61052B UDI-DI 10198459421587 Lot 26BBC156 DYNJT3266 UDI-DI 10198459320965 Lot 25LMH283 DYNJ0122428K UDI-DI 10198459533297 Lot 25EBP843A PHS656414I UDI-DI 10198459006258 Lot 25LMG515 DYNJ64949C UDI-DI 10198459190216 Lot 25LMH829 DYNJ83649B UDI-DI 10198459110177 Lot 25KBC046 DYNJ47104D UDI-DI 10198459624964 Lot 25LMJ846 DYNDA2664 UDI-DI 10193489342635 Lots 25JBT011 26CBD503 DYNJ84741B UDI-DI 10198459421563 Lot 25KBC487 DYNJ68253F UDI-DI 10198459185366 Lot 25KBA720 DYNJ83246B UDI-DI 10195327665463 Lots 25KBN031 25LBQ952 DYNJT6993 UDI-DI 10198459588211 Lot 25KBI629 DYNJ0509186J UDI-DI 10198459117626 Lot 25LMI076 CDS983181G UDI-DI 10198459038174 Lot 25LBA047

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 29 of 34

Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B

Z-2442-2026
Recall number
Z-2442-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJRA1739B UDI-DI 10195327411237 Lot 25LBB731

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 30 of 34

Medline convenience kits: PORT A CATH DYNJ906818A

Z-2443-2026
Recall number
Z-2443-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ906818A 10195327027261 25LBC291

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 31 of 34

Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR SURGICOUNT PACK DYNJ56573B ENDOVASCULAR PACK DYNJ29135N EP DEVICE DYNJ65916B FULL LINE ANEURYSM CDS CDS983672P GEN FEM POP #14-RF DYNJ21877W IMPLANT PACK DYNJ39316D OPEN HEART MRNGSD DYNJ58354F PACEMAKER PACK-LF DYNJ0618174N PACEMAKER SETUP PACK DYNJ35761D PACER / CATH LAB PACK-LF DYNJ0972604A PACER CDS CDS983686I PACER PACK DYNJ52059D PK, EP LAB PACEMAKER DYNJ43663A VENOUS ACCESS PACK DYNJ45640B

Z-2444-2026
Recall number
Z-2444-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

DYNJ58304B UDI-DI 10195327512699 Lot 25LBP470 DYNJ56573B UDI-DI 10193489903669 Lot 25KBK220 DYNJ29135N UDI-DI 10195327674755 Lot 25LMG563 DYNJ65916B UDI-DI 10193489902044 Lots 25KBG852 25LBB895 CDS983672P UDI-DI 10198459149139 Lots 25LBO027 26BBB852 DYNJ21877W UDI-DI 10195327104542 Lot 25JBW040 DYNJ39316D UDI-DI 10198459224447 Lot 25KBH774 DYNJ58354F UDI-DI 10195327515232 Lot 25KBI240 DYNJ0618174N UDI-DI 10195327227340 Lot 25KBC715 DYNJ35761D UDI-DI 10195327565374 Lot 26CBC772 DYNJ0972604A UDI-DI 10889942403905 Lot 25LMF965 CDS983686I UDI-DI 10193489852981 Lot 26ABE755 DYNJ52059D UDI-DI 10195327361785 Lots 25LBQ917 26CBE736 DYNJ43663A UDI-DI 10193489793680 Lot 26CBB662 DYNJ45640B UDI-DI 10193489494983 Lot 25LMJ305

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 32 of 34

Medline convenience kits: ADD-A-CATH ARTERIAL INSERTION ARTNC185 PED SCHOOL AGE PICC DRSG TRAY DYNDC3291

Z-2445-2026
Recall number
Z-2445-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

ARTNC185 UDI-DI 10195327640729 Lot 25JBU463 DYNDC3291 UDI-DI 10195327334741 Lot 25KBH082

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 33 of 34

Medline convenience kits: C SECTION CDS985505G C SECTION PACK DYNJ68260D C-SECTION DYNJ905094B C-SECTION RECOVERY #2 CDS820091P

Z-2446-2026
Recall number
Z-2446-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

CDS985505G UDI-DI 10195327412555 Lot 26AMC363 DYNJ68260D UDI-DI 10195327506513 Lot 25KBE168 DYNJ905094B UDI-DI 10193489858174 Lot 25KMB136 CDS820091P UDI-DI 10195327403539 Lots 26BBO404 26CBN891

Distribution pattern

US Nationwide distribution. OUS distribution pending.

device · product 34 of 34

Medline convenience kits: HYSTERECTOMY PACK-LF DYNJ20485L

Z-2447-2026
Recall number
Z-2447-2026
Initiated
April 27, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Medline Industries, LP
Quantity
49,654 kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Code information

UDI-DI 10195327024369 Lot 25LMJ031

Distribution pattern

US Nationwide distribution. OUS distribution pending.