Reported Jun 24, 2026 · Ongoing
MEDLINE Medical Procedure Kits labeled as: PELVIC LAP PACK, Medline Kit Number/ SKU DYNJ53820B
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 asPELVIC LAP PACK, Medline Kit Number/ SKU DYNJ53820B
- Lot codes and dates
UDI/DI 10195327548261 (each)40195327548262 (case)
- Lot Numbers
25LBI06225HBR96724JBK61824BBQ860
- Amount recalled
- 20 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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