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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 98862

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

Open FDA event record

Event summary

Timeline bucket
January 29, 2026
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
B Braun Medical Inc

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

8 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 8

Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY Model/Catalog Number: 555076 Software Version: N/A Product Description: CESK NORTHSIDE ANESTHESIA TRAY Component: No

Z-2263-2026
Recall number
Z-2263-2026
Initiated
January 29, 2026
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
280

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

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

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

Code information

Lot Code: Model No 555076, UDI-DI (Primary Device) 04046964313417, UDI-DI (Unit Device ID) 04046964313394, Lot Number 0062031523 Note: In the original customer notification (JAN2026), 280 pieces were distributed, to date, all pieces have been returned.

Distribution pattern

US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.

device · product 2 of 8

Brand Name: B. BRAUN MEDICAL INC. Product Name: BPSK, BLOCKJOCKS TRAY Model/Catalog Number: 570246 Software Version: N/A Product Description: BPSK, BLOCKJOCKS TRAY Component: No

Z-2264-2026
Recall number
Z-2264-2026
Initiated
January 29, 2026
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
210

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

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

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

Code information

Lot Code: Model No 570246, UDI-DI (Primary Device) 04046964526688, UDI-DI (Unit Device ID) 04046964526671, Lot Number 0062024481

Distribution pattern

US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.

device · product 3 of 8

Brand Name: B. BRAUN MEDICAL INC. Product Name: NES1725KFXL SPINAL EPID CLOSED TIP CATH Model/Catalog Number: 530201 Software Version: N/A Product Description: NES1725KFXL SPINAL EPID CLOSED TIP CATH Component: No

Z-2265-2026
Recall number
Z-2265-2026
Initiated
January 29, 2026
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
1730

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

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

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

Code information

Lot Code: Model No 530201, UDI-DI (Primary Device) 04046955672196, UDI-DI (Unit Device ID) 04046955672189, Lot Number 0062010965

Distribution pattern

US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.

device · product 4 of 8

Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model/Catalog Number: 555498 Software Version: N/A Product Description: CESK HARRIS METHODIST Component: No

Z-2266-2026
Recall number
Z-2266-2026
Initiated
January 29, 2026
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
690

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

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

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

Code information

Lot Code: Model No 555498, UDI-DI (Primary Device) 04046964315992, UDI-DI (Unit Device ID) 04046964315978, Lot Number 0062018999

Distribution pattern

US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.

device · product 5 of 8

Brand Name: B. BRAUN MEDICAL INC. Product Name: LYNDON B JOHNSON HOSPITAL SPINAL EPID Model/Catalog Number: 530184 Software Version: N/A Product Description: LYNDON B JOHNSON HOSPITAL SPINAL EPID Component: No

Z-2267-2026
Recall number
Z-2267-2026
Initiated
January 29, 2026
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
620

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

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

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

Code information

Lot Code: Model No 530184, UDI-DI (Primary Device) 04046955156528, UDI-DI (Unit Device ID) 04046955156511, Lot Number 0062019858

Distribution pattern

US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.

device · product 6 of 8

Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK RIVERSIDE HEALTH SYSTEM Model/Catalog Number: 552126 Software Version: N/A Product Description: CESK RIVERSIDE HEALTH SYSTEM Component: No

Z-2268-2026
Recall number
Z-2268-2026
Initiated
January 29, 2026
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
690

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

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

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

Code information

Lot Code: Model No 552126, UDI-DI (Primary Device) 04046955056903, UDI-DI (Unit Device ID) 04046955056897, Lot Number 0062031274

Distribution pattern

US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.

device · product 7 of 8

Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK SHANDS JACKSONVILLE 20055717 Model/Catalog Number: 555884 Software Version: N/A Product Description: CESK SHANDS JACKSONVILLE 20055717 Component: No

Z-2269-2026
Recall number
Z-2269-2026
Initiated
January 29, 2026
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
680

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

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

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

Code information

Lot Code: Model No 555884, UDI-DI (Primary Device) 04046964317361, UDI-DI (Unit Device ID) 04046964317347, Lot Number 0062036271

Distribution pattern

US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.

device · product 8 of 8

Brand Name: B. BRAUN MEDICAL INC. Product Name: SESK UPMC DOUBLE CATHETER TRAY Model/Catalog Number: 530134 Software Version: N/A Product Description: SESK UPMC DOUBLE CATHETER TRAY Component: No

Z-2270-2026
Recall number
Z-2270-2026
Initiated
January 29, 2026
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
390

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

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

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

Code information

Lot Code: Model No 530134, UDI-DI (Primary Device) 04046964305856, UDI-DI (Unit Device ID) 04046964305849, Lot Number 0062019148

Distribution pattern

US Nationwide distribution in the states of AL, FL, PA, TX, VA, WA.