AVID Medical recalls Halyard Angiography Pack Model MAMC218-18 due to potential metal flakes entering surgical sites. Affected units sold with specific lot numbers.
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
AVID Medical is recalling its Haly:Angiography Pack medical kits because small metal flakes could detach and enter surgical sites, causing reactions. This poses a risk of local reactions or foreign body reactions in patients during surgery.
The sponge forceps and towel clamps in the kit can release small metal flakes during use. These flakes may enter a patient's surgical site undetected, leading to local reactions or foreign body reactions.
Healthcare professionals using the Halyard Angiography Pack medical kits for procedures. Patients undergoing surgery with this kit are at risk of metal flakes entering surgical sites.
Check for the model number MAMC218-18 on the Halyard Angiography Pack. Affected units include specific lot numbers: 1591425 and 1597157.
Verify the model number MAMC218-18 and lot numbers 1591425 or 1597157 on the kit.
The recall indicates potential metal flakes could enter surgical sites, so it is not safe to use without recalling the product.
The recall does not specify a remedy, so contact AVID Medical for guidance.
Look for model number MAMC218-18 and lot numbers 1591425 or 1597157.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0412-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-0412-2025 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.
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.
