AVID Medical recalls Halyard SAMMC Angiography kit model SAMM066-15 due to potential risk of syringe rotating adaptor unwinding, causing loose or full disconnection between syringe and manifold.
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 its Halyard SAMMC Angiography kit (model SAMM066-15) because the syringe rotating adaptor may unwind during use, leading to loose or full disconnection between the syringe and manifold. This could cause medical complications during procedures.
The syringe rotating adaptor in the kit may unwind during use, causing a loose or full disconnection between the syringe and manifold. This could lead to medical complications if the connection is not secure during procedures.
Healthcare professionals using the Halyard SAMMC Angiography kit model SAMM066-15 are most at risk. The recall affects kits sold with specific lot numbers.
Check for the model number SAMM066-15 on the kit. Kits with lot numbers listed in the recall (e.g., 10809160388495, 1561685, etc.) are affected.
Verify the model number on the kit is SAMM066-15.
Reach out to AVID Medical for specific instructions on handling affected kits.
The recall indicates a potential risk of the syringe rotating adaptor unwinding, which could cause loose or full disconnection between the syringe and manifold, potentially leading to medical complications.
Check for the model number SAMM066-15 and lot numbers listed in the recall (e.g., 10809160388495, 1561685, etc.).
Contact AVID Medical for specific instructions on handling affected kits.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1978-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-1978-2026 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.
