Reported Jun 24, 2026 · Ongoing
MEDLINE Medical Procedure Kits labeled as BASIC GYN, CW LAP GYN, D&C HYSTEROSCOPY, CW LAP GYN, DEACONESS PELVIC LAP…
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 BASIC GYN, CW LAP GYN, D&C HYSTEROSCOPY, CW LAP GYN, DEACONESS PELVIC LAP PACK, FLOYD LAP GYN, GYN LAP PACK, GYN LAPAROSCOPY, GYN MINOR PACK, etc. (see the recall documents for a full list of affected products)
- Lot codes and dates
293 of 293 products
Products covered by this recall Model / number Barcodes Product as published DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 24GMJ742 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 24FMC978 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 24CMA556 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 24BMI027 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 24AMF247 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 24AMA807 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 23IMF051 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 23HMG141 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 23EMF259 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 23DMA689 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 23CMF097 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 23CMC699 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 22LME333 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 22KMB390 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 22HMC449 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 22GMD678 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 22FMG214 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 22DME100 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 22CME928 DYNJ905924B1019348977348440193489773485Medline Kit Number/ : UDI/DI 10193489773484 (each), 40193489773485 (case), Lot Number 22BMG698 - Amount recalled
- 44656 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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