Recall Z-1979-2026— AVID Medical, Inc.
Class I · Ongoing
Class I FDA medical device recall by AVID Medical, Inc., initiated 2026-03-13. FDA's recall record names no specific 510(k) clearance for this event. Product: Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.. Reason: 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..
- Recalling firm
- AVID Medical, Inc.
- Classification
- Class I
- Status
- Ongoing
- Initiated
- 2026-03-13
- Firm location
- Toano, VA, United States
Product description
Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.