fda_recall · device_recall · high

Medline Industries, LP — Class II recall: MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag, 14 Fr…

Event date
2026-06-24 00:00:00Z
Observed
2026-07-09 22:52:08Z
Source ID
Z-2483-2026
Payload hash
10718173837a35a715d9a3d9…

Summary

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… Status: Ongoing.

Entities

View source record ↗

Informational only. Not legal, financial, or medical advice.