FDA DevicesClass I
Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.
Published: May 13, 2026Recall ID: Z-1975-2026Category: devicesCountry: US
Reason for Recall / 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.
Product Description & Identification
Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.
Additional Source Details
| Field | Value |
|---|---|
| City | Toano |
| State | VA |
| Event id | 98686 |
| Address 1 | 9000 Westmont Dr |
| Code info | Model Number: SELF131-05. UDI-DI (Kit Lot Numbers): 10809160408650 (1611688, 1611689, 1618351, 1621441, 1627930, 1635908, 1644501, 1646021, 1651957, 1654887, 1656582, 1656581, 1659713, 1670884, 1670885, 1671950). |
| Postal code | 23168-9351 |
| Report date | 20260513 |
| Product type | Devices |
| Product quantity | 2,932 kits |
| Reason for recall | 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. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260313 |
| Initial firm notification | |
| Center classification date | 20260501 |
Overview
- Recalling FirmAVID Medical, Inc.
- StatusOngoing
- Risk LevelClass I
- DistributionUS distribution to FL, IL, MO, MS, NC, NE, TX.