AVID Medical recalls Halyard ANG: 004-01 medical kits due to metal flakes potentially entering surgical sites. Affected units include specific model and lot numbers. Contact for remedy.
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 ANGIO ARTERIOGRAM PACK medical kits (model MMCC004-01) because small metal flakes could detach and enter surgical sites, causing reactions or infections. This risk affects patients during procedures using these kits.
The kits contain sponge forceps and towel clamps that may shed small metal flakes during use. These flakes can enter a patient's surgical site without detection, leading to local reactions or foreign body reactions.
Healthcare professionals using the Halyard ANGIO ARTERIOGRAM PACK kits for medical procedures are most at risk. Patients undergoing surgery with these kits could face complications from undetected metal flakes.
Check for model number MMCC004-01 on the Halyard ANGIO ARTERIOGRAM PACK kits. Affected lots include 1605588 and 1605589. The kits were sold with GTIN 10809160421772.
Identify the model number on the kit, which should be MMCC004-01 for affected units.
Reach out to AVID Medical for guidance on next steps as the recall remedy is not specified.
The recalled model number is MMCC004-01.
Affected lots are 1605588 and 1605589.
The recall remedy is not specified in the record, so contact AVID Medical for instructions.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0414-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-0414-2025 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.
