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FDAFDA · Food and drugs·Recall number Z-2180-2026

BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Published May 20, 2026 · Recall initiated: April 10, 2026

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Incomplete seals on sterile product

What to do

Voluntary: Firm initiated

Recall details

Manufacturer
Stryker Sustainability Solutions
Distributor
US Nationwide and the countries of Israel and Canada.
Lot
UDI 00885825003890, Lot Numbers: 4064760, 4336810, 4381356, 4381359, 4401919.
Risk classification
Class II
Area (FDA)
device
Country
United States

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