AVID Medical recalls Halyard IR Biopsy Pack Model AVMD019-01 due to potential metal flakes entering surgical sites. Affected units sold with lot number 1583034.
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 Halyard IR Biopsy Packs (model AVMD019-01) because small metal flakes could detach and enter surgical sites, causing reactions or foreign body issues. This affects medical devices used during procedures.
The sponge forceps and towel clamps in the biopsy pack can release small metal flakes during use. These flakes may enter the surgical site undetected, leading to local reactions or foreign body reactions in patients.
Medical professionals using the Halyard IR Biopsy Pack for surgical procedures are most at risk. Patients undergoing surgery with this device may experience local reactions or foreign body reactions.
Check for the model number AVMD019-01 on the Halyard IR Biopsy Pack. Units sold with lot number 1583034 are affected. The product is a medical convenience kit for surgical procedures.
Look for model number AVMD019-01 and lot number 1583034 on the Halyard IR Biopsy Pack.
Yes, metal flakes could enter surgical sites causing local reactions or foreign body reactions.
Check for model number AVMD019-01 and lot number 1583034 on the Halyard IR Biopsy Pack.
The recall does not specify a remedy, so contact AVID Medical for 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-0384-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-0384-2025 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.