Recall
FDAHealthMay 4, 2026

Medline Industries, LP — MEDLINE Pre-connected Urethral Catheterization Tray and Bag, Red Rubber Latex, 15 Fr, Medline Product Number/SKU (REF) DYND10407

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
May 4, 2026

Worldwide distribution - US Nationwide and the countries of AE, BB, BM, BS, CA, CY, GU, NL, PA, QA, SA, VI.

What's affected?

Product
MEDLINE Pre-connected Urethral Catheterization Tray and Bag, Red Rubber Latex, 15 Fr, Medline Product Number/SKU (REF) DYND10407
Lot code
S

Additional details

UDI/DI 10080196990740 (each), 40080196990741 (case); ALL LOTS

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 4304669 units.

View original FDA notice →

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