Reported Jun 24, 2026 · Ongoing
MEDLINE Medical Procedure Kits labeled as: 1) KIT UROLOGY URETHROPLASTY, Medline Kit Number/SKU DYKMBNDL117C; 2)…
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
1) KIT UROLOGY URETHROPLASTYMedline Kit Number/SKU DYKMBNDL117C2) URETHROPLASTYMedline Kit Number/SKU DYNJ9089783) URETHROPLASTYMedline Kit Number/SKU DYNJ908978F
- Lot codes and dates
8 of 8 products
Products covered by this recall Model / number Barcodes Product as published DYKMBNDL117C1019532737110440195327371105Medline Kit Number/ : UDI/DI 10195327371104 (each), 40195327371105 (case), Lot Number 23DLA834 DYNJ9089781019532723113240195327231133Medline Kit Number/ : UDI/DI 10195327231132 (each), 40195327231133 (case), Lot Number 23BMC463 DYNJ9089781019532723113240195327231133Medline Kit Number/ : UDI/DI 10195327231132 (each), 40195327231133 (case), Lot Number 23AMA685 DYNJ9089781019532723113240195327231133Medline Kit Number/ : UDI/DI 10195327231132 (each), 40195327231133 (case), Lot Number 23AMB905 DYNJ9089781019532723113240195327231133Medline Kit Number/ : UDI/DI 10195327231132 (each), 40195327231133 (case), Lot Number 22LMG466 DYNJ9089781019532723113240195327231133Medline Kit Number/ : UDI/DI 10195327231132 (each), 40195327231133 (case), Lot Number 22LMB983 DYNJ908978F1019845922880340198459228804Medline Kit Number/ : UDI/DI 10198459228803 (each), 40198459228804 (case), Lot Number 25JBD225 DYNJ908978F1019845922880340198459228804Medline Kit Number/ : UDI/DI 10198459228803 (each), 40198459228804 (case), Lot Number 25HBW236. - Amount recalled
- 91 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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