AVID Medical recalls Halyard CARDIAC CATH PACK kits with model EAMC1000-05 or WAFB208-02 due to potential syringe disconnection during use. Affected units may have loose connections causing medical issues.
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 specific Halyard CARDIAC CATH PACK kits that could cause the syringe to disconnect from the manifold during use. This poses a risk of medical complications if the connection becomes loose.
The syringe rotating adaptor in the kit may unwind during use, leading to a loose or full disconnection between the syringe and manifold. This could cause medical complications if the connection is not secure during treatment.
Healthcare professionals using the Halyard CARDIAC CATH PACK kits for medical procedures are most at risk. Patients receiving treatments with these kits may also be affected if the connection becomes loose.
Check for model numbers EAMC1000-05 (with specific lot numbers) or WAFB208-02 (with specific lot numbers) on the kit packaging or label.
Identify the model number on the kit (EAMC1000-05 or WAFB208-02) and compare with the listed lot numbers to confirm if it is affected.
The recall is due to a potential risk of the syringe rotating adaptor unwinding during use, which could cause a loose or full disconnection between the syringe and manifold.
Check the model number and lot numbers to see if it is affected. If it is, contact AVID Medical for further instructions.
The recall record does not mention a specific fix or remedy for this issue.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1970-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-1970-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
