Reported Jun 24, 2026 · Ongoing

MEDLINE Medical Procedure Kits labeled as

Medline Industries, LP

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

MEDLINE Medical Procedure Kits labeled as

50 of 50 products

Products covered by this recall
Model / numberProduct as published
DYNJ63789ACHEST EXPLORATION ECMO, Medline Kit Number/
DYNJ17321GCORONARY/ARTERY BYPASS TRAY, Medline Kit Number/
DYNJ909989BD&C/CYSTO, Medline Kit Number/
DYNJ53214DDD LAPAROSCOPY PACK, Medline Kit Number/
DYNJ903390KDIAGNOSTIC LAPAROSCOPY, Medline Kit Number/
DYNJ902700CGENERAL LAPAROSCOPY, Medline Kit Number/
DYNJ902700DGENERAL LAPAROSCOPY, Medline Kit Number/
DYNJ902700FGENERAL LAPAROSCOPY, Medline Kit Number/
DYNJ64324AGENERAL-CVOR MINOR, Medline Kit Number/
DYNJT7061GYN LAP, Medline Kit Number/
DYNJ53631FGYN LAPAROSCOPY PACK, Medline Kit Number/
DYNJ85910GYN MINOR PACK, Medline Kit Number/
DYKMBNDL117AKIT UROLOGY URETHROPLASTY, Medline Kit Number/
DYNJ904585BLAP, Medline Kit Number/
DYNJ904585CLAP, Medline Kit Number/
CDS983255RLAP CHOLE CDS, Medline Kit Number/
CDS983255SLAP CHOLE CDS, Medline Kit Number/
CDS983255TLAP CHOLE CDS, Medline Kit Number/
DYNJ89908LAPAROSCOPY, Medline Kit Number/
DYNJ910517LAPAROSCOPY, Medline Kit Number/
Lot codes and dates

305 of 305 products

Products covered by this recall
#BarcodesProduct as published
11019845914977140198459149772UDI/DI 10198459149771 (each), 40198459149772 (case), Lot Number 26BBD116
21019845914977140198459149772DYNJ63789A: UDI/DI 10198459149771 (each), 40198459149772 (case), Lot Number 26ABL500
31019845914977140198459149772DYNJ63789A: UDI/DI 10198459149771 (each), 40198459149772 (case), Lot Number 25FBH410
41019845914977140198459149772DYNJ63789A: UDI/DI 10198459149771 (each), 40198459149772 (case), Lot Number 25EBQ051
51019845914977140198459149772DYNJ63789A: UDI/DI 10198459149771 (each), 40198459149772 (case), Lot Number 25DBS969
61019845914977140198459149772DYNJ63789A: UDI/DI 10198459149771 (each), 40198459149772 (case), Lot Number 24LBQ812
71019845914977140198459149772DYNJ63789A: UDI/DI 10198459149771 (each), 40198459149772 (case), Lot Number 24LBF658
81019845914977140198459149772DYNJ63789A: UDI/DI 10198459149771 (each), 40198459149772 (case), Lot Number 24JBM406
91019348932386340193489323864DYNJ17321G: UDI/DI 10193489323863 (each), 40193489323864 (case), Lot Number 23GBM492
101019348932386340193489323864DYNJ17321G: UDI/DI 10193489323863 (each), 40193489323864 (case), Lot Number 22IBV269
111019348932386340193489323864DYNJ17321G: UDI/DI 10193489323863 (each), 40193489323864 (case), Lot Number 22HBV981
121019348932386340193489323864DYNJ17321G: UDI/DI 10193489323863 (each), 40193489323864 (case), Lot Number 22HBF916
131019845932268640198459322687DYNJ909989B: UDI/DI 10198459322686 (each), 40198459322687 (case), Lot Number 25GBW197
141019845932268640198459322687DYNJ909989B: UDI/DI 10198459322686 (each), 40198459322687 (case), Lot Number 25GBD634
151019845932268640198459322687DYNJ909989B: UDI/DI 10198459322686 (each), 40198459322687 (case), Lot Number 25FBB533
161019845932268640198459322687DYNJ909989B: UDI/DI 10198459322686 (each), 40198459322687 (case), Lot Number 25EBC752
171088994238830140889942388302DYNJ53214: UDI/DI 10889942388301 (each), 40889942388302 (case), Lot Number 21HMG546
181088994238830140889942388302DYNJ53214: UDI/DI 10889942388301 (each), 40889942388302 (case), Lot Number 21HMC179
191019845952282640198459522827DYNJ903390K: UDI/DI 10198459522826 (each), 40198459522827 (case), Lot Number 26ABQ562
201019845952282640198459522827DYNJ903390K: UDI/DI 10198459522826 (each), 40198459522827 (case), Lot Number 25JBB643
Amount recalled
10415 units

This recall covers 64 products

The agency filed one notice per product. You are reading one of them; the other 63 are below.

51 more are in the archive.

Where it was sold

Why it was recalled

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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By hazard

Other recalls from Medline Industries, LP

36 in total.

Where it was distributed

All recall categories · Browse the whole archive

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:32 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.