Recall Z-2498-2026

Recall number
Z-2498-2026
Event number
98994
Firm FEI
1417592
Product code
MCY
Status
Open, Classified
Initiated
2026-05-04
Posted
2026-06-17
Root cause
Nonconforming Material/Component
510(k) numbers
K963719, K931932, K923905, K924690, K970721, K905123, K960585, K905572, K926063, K951022, K912116, K951021, K910363, K912232, K921347, K902811, K952334, K951476, K910011, K912684, K912117, K913480, K925021, K913479

Product#

MEDLINE Medical Procedure Kits labeled as: DR FERNANDEZ, Medline kit number/SKU DYNJ68808

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.