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Medical Device

BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER

Recall date: 2026-05-20 · Source: FDA_DEVICE
Brand / Firm
Stryker Sustainability Solutions
Product
BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Reason for recall
Incomplete seals on sterile product
Units affected
90 units
Description
BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER
View official recall notice →