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Recall Observatory FDA recall evidence

Device product

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

Z-2481-2026

May 04, 2026

Class II

Product summary

Firm
Medline Industries, LP
Event
Event 98994
Status
Ongoing
Classification
Class II
Quantity
4304669 units
Official record key
device-enforcement:Z-2481-2026

Official wording

Reason: 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.

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

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.