Recall Z-2491-2026
- Recall number
- Z-2491-2026
- Event number
- 98994
- Firm FEI
- 1417592
- Product code
- OGR
- Status
- Open, Classified
- Initiated
- 2026-05-04
- Posted
- 2026-06-17
- Root cause
- Nonconforming Material/Component
Product#
MEDLINE Medical Procedure Kits labeled as: ADULT TRACHEOSTOMY TUBE INSERT, ASC T&A, CONWAY T&A SINUS, EAR PACK, etc. (see the recall documents for the full list of products)
Reason for Recall#
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.