← All recalls
Medical Device

BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Recall date: 2026-05-20 · Source: FDA_DEVICE
Brand / Firm
Stryker Sustainability Solutions
Product
BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Reason for recall
Incomplete seals on sterile product
Units affected
44 units
Description
BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER
View official recall notice →