- Recalling firm
- AVID Medical, Inc.
- 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.
- Affected products (lot / model / serial)
- Model Number: VMCD029. UDI-DI (Kit Lot Numbers): 10809160388969 (1601753, 1601754, 1621560).
- Units affected
- 75 kits
- Distribution pattern
- US distribution to FL, IL, MO, MS, NC, NE, TX.
- Firm location
- Toano, VA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1979-2026
- Recall initiated
- March 13, 2026
- FDA classification date
- May 1, 2026
- FDA report date
- May 13, 2026
- FDA event ID
- 98686
- Last updated on HTM Vibe
- July 24, 2026