FDA recall Z-2178-2026
Stryker Sustainability Solutions · Class II · device
Product
BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Reason for recall
Incomplete seals on sterile product
Distribution
US Nationwide and the countries of Israel and Canada.
Key facts
- Status
- Ongoing
- Initiation date
- 2026-04-10
- Report date
- 2026-05-20
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Tempe, AZ, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2178-2026