Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | High |
| Status | ongoing |
| Recall date | March 13, 2026 |
| Reported | May 13, 2026 |
| Recalling firm | AVID Medical, Inc. |
| Country / region | United States VA |
Hazard
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Affected products
- Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
Related recalls
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