AVID Medical recalls Halyard VA Detroit Cath Lab Pack kit (model VMCD029) due to potential syringe disconnection during use. Affected units may cause medical complications if not addressed.
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.
AVID Medical is recalling Halyard VA Detroit Cath Lab Pack kits with model number VMCD029 because the syringe rotating adaptor might unwind, causing a loose or full disconnection between the syringe and manifold. This could lead to medical complications if the kit is used without proper connection.
The syringe rotating adaptor may unwind during use, leading to a loose or full disconnection between the syringe and manifold. This could cause medical complications if the kit is used without a secure connection.
Healthcare professionals using the Halyard VA Detroit Cath Lab Pack kit with model VMCD029 are most at risk. Patients receiving care with this kit could be affected if the connection becomes loose or disconnected.
Check for the model number VMCD029 on the Halyard VA Detroit Cath Lab Pack kit. Units sold with lot numbers 10809160388969 (1601753, 1601754, 1621560) are affected.
Verify the model number on the kit; affected units have VMCD029.
If the kit is in use, confirm the syringe rotating adaptor is not unwinding to prevent disconnection.
The model number is VMCD029.
Check for the model number VMCD029 and lot numbers 10809160388969 (1601753, 1601754, 1621560).
Ensure the syringe rotating adaptor is secure to prevent disconnection; contact AVID Medical for further instructions.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1979-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-1979-2026 from AVID Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
