Recall events
/
Event 95393
Event summary
Timeline bucket August 28, 2024
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording MEDLINE INDUSTRIES, LP - Northfield
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
6 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 6
MEDLINE HEART CABG CDS, REF CDS983376R
Z-0119-2025
Recall number Z-0119-2025
Initiated August 28, 2024
Classification Class II
Status Ongoing
Quantity 15 kits
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
incorrectly labeled
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0119-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23125]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
Code information UDI/DI 40195327548545 (case), 10195327548544 (each), Lot Numbers: 24BMF012, 24CMG491
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[4373]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 6
MEDLINE HEART OVERHEAD TABLE PACK, REF DYNJ0778508J
Z-0120-2025
Recall number Z-0120-2025
Initiated August 28, 2024
Classification Class II
Status Ongoing
Quantity 60 kits
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
incorrectly labeled
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0120-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5328]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
Code information UDI/DI 40195327563784 (case), 10195327563783 (each), Lot Numbers: 24BMD381, 24BMJ452
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[4110]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 6
MEDLINE OPEN HEART PACK, REF DYNJ66216C
Z-0121-2025
Recall number Z-0121-2025
Initiated August 28, 2024
Classification Class II
Status Ongoing
Quantity 123 kits
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
incorrectly labeled
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0121-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[28675]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
Code information UDI/DI 40193489853361 (case), 10193489853360 (each), Lot Numbers: 23LBM368, 23LBH354
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[4267]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 6
MEDLINE OPEN HEART, REF DYNJ904261B
Z-0122-2025
Recall number Z-0122-2025
Initiated August 28, 2024
Classification Class II
Status Ongoing
Quantity 30 units
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
incorrectly labeled
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0122-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5322]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
Code information UDI/DI 40193489479530 (case), 10193489479539 (each), Lot Numbers: 23LBR364
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[4195]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 6
MEDLINE KIT CV I II, REF DYNJ906071B
Z-0123-2025
Recall number Z-0123-2025
Initiated August 28, 2024
Classification Class II
Status Ongoing
Quantity 56 kits
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
incorrectly labeled
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0123-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[40700]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
Code information UDI/DI 40195327227235 (case), 10195327227234 (each), Lot Numbers: 24ABA223
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[4186]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 6
MEDLINE OPEN HEART NIMC KIT, REF DYNJ908840
Z-0124-2025
Recall number Z-0124-2025
Initiated August 28, 2024
Classification Class II
Status Ongoing
Quantity 22 kits
App-derived interpretation
Labeling or packaging
reason.labeling_packaging · v1.0.0
incorrectly labeled
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0124-2025
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57889]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
Code information UDI/DI 40195327185078 (case), 10195327185077 (each), Lot Numbers: 24BMF235
Distribution pattern US Nationwide distribution.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[38022]
FDA event record
· Exact recall-number query on openFDA
