FDAClass I · Medical device · Recalled May 13, 2026
Halyard PERC TRAY kit recall — AVID Medical, Inc.
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.
Class I: most serious — reasonable probability of serious health consequences or death.
View the official FDA enforcement record (openFDA) ↗
- Official recall ID
- Z-1977-2026
- Brand
- AVID Medical
- Classification
- Class I
- Units affected
- 6,052 kits
- Recall status
- Ongoing
- Initiated
- Voluntary: Firm initiated
Description
Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.
Affected products
Companies & origin
- Recalling firm location
- Toano, VA, United States
- Firm address
- 9000 Westmont Dr, 23168-9351
Identifying details (verbatim from the notice)
- Product codes / lots
- 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).
- Distribution
- US distribution to FL, IL, MO, MS, NC, NE, TX.
- Firm notified the public via
- E-Mail
- FDA event ID
- 98686
- Recall initiated
- March 13, 2026
- FDA classified
- May 1, 2026
- FDA report date
- May 13, 2026
Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim;
the linked government source is authoritative. Source last checked July 24, 2026 at 3:00 AM UTC.
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