BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER
USBARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Recalling Firm: Stryker Sustainability Solutions
Reason for Recall / Hazard
Incomplete seals on sterile product
Product Description & Identification
BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Additional Source Details
| Field | Value |
|---|---|
| City | Tempe |
| State | AZ |
| Event id | 98708 |
| Address 1 | 1810 W Drake Dr |
| Code info | UDI 00885825003876, Lot Numbers: xxxxx |
| Postal code | 85283-4327 |
| Report date | 20260520 |
| Product type | Devices |
| Reason for recall | Incomplete seals on sterile product |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260410 |
| Center classification date | 20260513 |
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Overview
- Recalling FirmStryker Sustainability Solutions
- StatusOngoing
- Risk LevelClass II
- DistributionUS Nationwide and the countries of Israel and Canada.
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🚨 SAFETY ALERT: Stryker Sustainability Solutions - BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER Check if your household is affected: https://therecallfile.com/recalls/bard-dynamic-xt-steerable-product-number-201103-reprocessed-electrophy/FDA-Z-2179-2026
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