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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