AVID Medical recalls Halyard Suture Pack CABG kits with potential silicone coating loss during use. Affected models include SILV800-01, lot 1642454, expiring 2/4/2028. No immediate action needed but check for coating issues.
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
AVID Medical is recalling Halyard Suture Pack CABG kits due to possible loss of silicone coating on surgical needles during use. This could lead to diminished performance or needle removal, but the risk is not severe enough to require immediate stoppage.
The surgical needles in these kits may lose their silicone coating during use, which could reduce performance or cause the needle to become loose. This is a material issue but does not typically lead to serious injury or death.
Surgical professionals and hospitals using the Halyard Suture Pack CABG kit with model SILV800-01, lot 1642454, expiring 2/4/2028. The risk is low for most users as the coating issue is unlikely to cause serious injury.
Check for the model number SILV800-01 on the kit, lot code 1642454, and expiration date 2/4/2028. The product is sold by AVID Medical.
Verify the model number, lot code, and expiration date on the Halyard Suture Pack CABG kit.
No, the recall is for potential coating loss during use, which may reduce performance but does not typically cause serious injury.
No immediate action is required. The recall does not mandate stopping use, only checking for coating issues.
Check the model number, lot code, and expiration date. If it matches, contact AVID Medical for further guidance.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1742-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-1742-2025 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.
