Reported Jun 24, 2026 · Ongoing
MEDLINE Medical Procedure Kits labeled as: KIT URO ROBOT CYSTECTOMY, D AND C PACK, MAD D & C, VPH LITHOTOMY MINOR,…
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 asKIT URO ROBOT CYSTECTOMY, D AND C PACK, MAD D & C, VPH LITHOTOMY MINOR, TRMC- PERI GYN PACK, RICH MINOR LITHOTOMY, etc. (see recall documents for a full list of products)
- Lot codes and dates
294 of 294 products
Products covered by this recall Model / number Barcodes Product as published DYNJ83242B1019845915702840198459157029Medline Kit Number/ : UDI/DI 10198459157028 (each), 40198459157029 (case), Lot Number 25HBR321 DYNJ83242B1019845915702840198459157029Medline Kit Number/ : UDI/DI 10198459157028 (each), 40198459157029 (case), Lot Number 25GBD202 DYNJ83242B1019845915702840198459157029Medline Kit Number/ : UDI/DI 10198459157028 (each), 40198459157029 (case), Lot Number 25FBK813 DYNJ83242B1019845915702840198459157029Medline Kit Number/ : UDI/DI 10198459157028 (each), 40198459157029 (case), Lot Number 25EBG207 DYNJ61059B1019532719345440195327193455Medline Kit Number/ : UDI/DI 10195327193454 (each), 40195327193455 (case), Lot Number 23FBK499 DYNJ61059B1019532719345440195327193455Medline Kit Number/ : UDI/DI 10195327193454 (each), 40195327193455 (case), Lot Number 23EBV071 DYNJ61059B1019532719345440195327193455Medline Kit Number/ : UDI/DI 10195327193454 (each), 40195327193455 (case), Lot Number 22KBK089 DYNJ61059B1019532719345440195327193455Medline Kit Number/ : UDI/DI 10195327193454 (each), 40195327193455 (case), Lot Number 22IBV707 DYNJ61059B1019532719345440195327193455Medline Kit Number/ : UDI/DI 10195327193454 (each), 40195327193455 (case), Lot Number 22HBC310 DYNJ61059C1019532745165340195327451654Medline Kit Number/ : UDI/DI 10195327451653 (each), 40195327451654 (case), Lot Number 26DMG168 DYNJ61059C1019532745165340195327451654Medline Kit Number/ : UDI/DI 10195327451653 (each), 40195327451654 (case), Lot Number 26CMD637 DYNJ61059C1019532745165340195327451654Medline Kit Number/ : UDI/DI 10195327451653 (each), 40195327451654 (case), Lot Number 25KMC849 DYNJ61059C1019532745165340195327451654Medline Kit Number/ : UDI/DI 10195327451653 (each), 40195327451654 (case), Lot Number 25JMA672 DYNJ61059C1019532745165340195327451654Medline Kit Number/ : UDI/DI 10195327451653 (each), 40195327451654 (case), Lot Number 25DMC189 DYNJ61059C1019532745165340195327451654Medline Kit Number/ : UDI/DI 10195327451653 (each), 40195327451654 (case), Lot Number 25CMH655 DYNJ61059C1019532745165340195327451654Medline Kit Number/ : UDI/DI 10195327451653 (each), 40195327451654 (case), Lot Number 25CMC735 DYNJ61059C1019532745165340195327451654Medline Kit Number/ : UDI/DI 10195327451653 (each), 40195327451654 (case), Lot Number 24KMA168 DYNJ61059C1019532745165340195327451654Medline Kit Number/ : UDI/DI 10195327451653 (each), 40195327451654 (case), Lot Number 24IMD969 DYNJ61059C1019532745165340195327451654Medline Kit Number/ : UDI/DI 10195327451653 (each), 40195327451654 (case), Lot Number 24GMF018 DYNJ61059C1019532745165340195327451654Medline Kit Number/ : UDI/DI 10195327451653 (each), 40195327451654 (case), Lot Number 24EMA387 - Amount recalled
- 32438 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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