AVID Medical recalls Halyard Total Knee kits (model EUOR002-06) due to potential metal flakes entering surgical sites. Affected kits may cause local reactions or foreign body reactions.
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 Total Knee medical convenience kits with model number EUOR00:06 because small metal flakes could detach and enter surgical sites, potentially causing reactions or foreign body issues.
Small metal flakes could detach from the kit components and enter a patient's surgical site undetected. This might cause local reactions or foreign body reactions, though the risk is low.
Medical professionals using the Halyard Total Knee kits with model EUOR002-06 are most at risk. Patients who have undergone knee surgery with these kits may also be affected.
Check for the model number EUOR002-06 on the Halyard Total Knee kits. The kits were sold with lot number 1611448.
Look for the model number EUOR002-06 on the Halyard Total Knee kits.
The recall is due to small metal flakes potentially detaching from the kit components and entering surgical sites, which could cause local reactions or foreign body reactions.
Check the model number on the kit. If it's EUOR002-06, contact AVID Medical for further instructions.
The recall notes potential for local reactions or foreign body reactions, but does not specify serious injury risks.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0395-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-0395-2025 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.
