Daig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | Medium |
| Status | ongoing |
| Recall date | April 10, 2026 |
| Reported | May 20, 2026 |
| Recalling firm | Stryker Sustainability Solutions |
| Country / region | United States AZ |
Hazard
Incomplete seals on sterile product
Affected products
- Daig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER
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