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Medline Red Rubber Latex Urethral Catheter
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MEDICAL DEVICE RECALLMODERATE

Medline Red Rubber Latex Urethral Catheter

Medline recalls Red Rubber Latex Urethral Catheters over surface finish and connector issues.

What to do

Inspect your inventory for the affected REF numbers and discontinue use immediately. Contact Medline for return and replacement instructions.

Posted
Updated
Recall No.
Z-2480-2026
Agency
Firm
Medline Industries, LP
Recall ID
98994
Status
ONGOING

Why it was recalled

Medline Industries is recalling its Red Rubber Latex Urethral Catheters due to irregularities in surface finish, premature connector detachment, and out-of-specification outer diameters. The affected products include 11 SKUs in French sizes 8 Fr through 22 Fr.

Is mine affected?

This recall covers 34 products. Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

ProductUPCRecall #
MEDLINE Medical Procedure Kits labeled as10195327191887, 40195327191888, 10195327191887, 40195327191888, 10195327287764, 40195327287765, 10195327287764, 40195327287765, 10195327287764, 40195327287765, 10195327432119, 40195327432110, 10195327432119, 40195327432110, 10195327432119, 40195327432110, 10195327432119, 40195327432110, 10195327432119, 40195327432110Z-2496-2026
MEDLINE Medical Procedure Kits labeled as: 1) BASIC HEART PACK, Medline Kit/SKU DYNJ67331B; 2) CARDIAC SURGERY, Medline Kit/SKU DYNJ911589A; 3) CAROTID ENDARTECOMY, Medline Kit/SKU DYNJ36211D; 4) CHLA ECMO / CARDIAC PACK, Medline Kit/SKU DYNJ87973; 5) CHLA ECMO / CARDIAC PACK, Medline Kit/SKU DYNJ87973A; 6) CV PART 1 AND 2, Medline Kit/SKU DYNJ908879; 7) CV PART 1 AND 2, Medline Kit/SKU DYNJ908879C; 8) FEM POP CDS, Medline Kit/SKU CDS983670K; 9) LAP BASIN TRAY, Medline Kit/SKU10195327013837, 40195327013838, 10195327013837, 40195327013838, 10195327013837, 40195327013838, 10195327013837, 40195327013838, 10195327013837, 40195327013838, 10195327013837, 40195327013838, 10195327013837, 40195327013838, 10195327013837, 40195327013838, 10195327013837, 40195327013838, 10195327013837, 40195327013838Z-2486-2026
MEDLINE Medical Procedure Kits labeled as CH OPEN HEART, ADULT CARDIAC KIT, AHT CVOR CABG, APH EMERGENCY OPEN HEART PACK, Etc. (see recall documents for a full list of products)10193489344240, 40193489344241, 10193489847123, 40193489847124, 10193489847123, 40193489847124, 10193489847123, 40193489847124, 10193489847123, 40193489847124, 10193489847123, 40193489847124, 10193489847123, 40193489847124, 10193489847123, 40193489847124, 10193489847123, 40193489847124, 10193489847123, 40193489847124Z-2487-2026
MEDLINE Medical Procedure Kits labeled as: LAPAROSCOPY COMBINED - NO NDL, Medline Kit Number/SKU DYNJ37378A10889942113583, 40889942113584Z-2485-2026
MEDLINE Medical Procedure Kits labeled as: PELVIC LAP PACK, Medline Kit Number/ SKU DYNJ53820B10195327548261, 40195327548262Z-2502-2026
MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY, CSC-N PELVISCOPY, D AND C PACK, D&C HYSTER PACK, FLWR GYN PACK, FS LAP TUBAL LIGATION, HILLSDALE D&C / HYSTEROSCOPY, LAVH NEW BRAUNFELS,TVH PACK, etc (see recall documents for a full list of affected products)10193489640458, 40193489640459, 10195327193478, 40195327193479, 10195327193478, 40195327193479, 10195327193478, 40195327193479, 10195327193478, 40195327193479, 10195327451684, 40195327451685, 10195327451684, 40195327451685, 10195327451684, 40195327451685, 10195327451684, 40195327451685, 10195327451684, 40195327451685Z-2505-2026
MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag, 16 Fr, 1000mL, Medline Product Number/SKU (REF) URO4RR16C10197344149001, 20197344149008Z-2484-2026
MEDLINE Medical Procedure Kits labeled as: CATH 22F ROBINSON STRL 5'S PK, Medline Kit Number/SKU DYNJ004083910889942046126, 40889942046127Z-2492-2026

+26 more affected products. See the full list at the official source below.

Where it was sold

Distributed nationwide.

Other recent recalls from Medline Industries, LP

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Editorial summary by Recall Canary · last updated 2026-07-28 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification