← FDA ENFORCEMENT
Z-1977-2026Class I

AVID Medical, Inc.

Recalling firm
AVID Medical, Inc.
Product type
Device
Status
Ongoing
Report date
2026-05-13
Distribution
US distribution to FL, IL, MO, MS, NC, NE, TX.
Firm state
VA
Product quantity
6,052 kits
Initiated by
Voluntary: Firm initiated
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.

Product description

Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.

Code / lot info

1. Model Number: SLPC34-01. UDI-DI (Kit Lot Numbers): 10809160450963 (1640169, 1641409, 1641410, 1641411, 1641412, 1641413, 1641414, 1641415, 1645684); 10809160459904 (1649576, 1660882, 1660883, 1660884, 1663896, 1665768). 2. Model Number: SLPC34-02. UDI-DI (Kit Lot Numbers): DHR 108916049515 NAV 10809160511213 (1668809, 1668810, 1668812, 1668813, 1668814, 1668815, 1668816).

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.