Z-2180-2026 Class II Ongoing
FDA device recall Z-2180-2026 was initiated by Stryker Sustainability Solutions on April 10, 2026 and is designated Class II. Reason for recall: Incomplete seals on sterile product The recall status is ongoing. Affected quantity: 5 units.
Recall Details
- Product Type
- Devices
- Report Date
- May 20, 2026
- Initiation Date
- April 10, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5 units
Product Description
BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Reason for Recall
Incomplete seals on sterile product
Distribution Pattern
US Nationwide and the countries of Israel and Canada.
Code Information
UDI 00885825003890, Lot Numbers: 4064760, 4336810, 4381356, 4381359, 4401919.