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 / numberBarcodesProduct 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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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:43 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.