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Recall Observatory FDA recall evidence

Device product

MEDLINE Medical Procedure Kits labeled as: PELVIC LAP PACK, Medline Kit Number/ SKU DYNJ53820B

Z-2502-2026

May 04, 2026

Class II

Product summary

Firm
Medline Industries, LP
Event
Event 98994
Status
Ongoing
Classification
Class II
Quantity
20 units
Official record key
device-enforcement:Z-2502-2026

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 10195327548261 (each), 40195327548262 (case). Lot Numbers: 25LBI062, 25HBR967, 24JBK618, 24BBQ860.

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.