AVID Medical recalls Halyard C SECTION BUNDLE medical kits with model LANC015-34 due to potential metal flakes causing surgical site reactions. 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 medical convenience kits (Halyard C SECTION BUNDLE) model LANC01:34 because small metal flakes could detach and enter surgical sites, causing reactions or infections. This poses a risk to patients during surgery.
The sponge forceps and towel clamps in the kit may release small metal flakes during use. These flakes can enter a patient's surgical site without being noticed, leading to local reactions or foreign body reactions.
Medical professionals using the Halyard C SECTION BUNDLE kits during surgery are most at risk. Patients undergoing procedures with these kits could face complications from undetected metal flakes.
Check for the model number LANC015-34 on the kit. Affected units were sold with lot numbers 1590497 or 1601534.
Look for model number LANC015-34 on the Halyard C SECTION BUNDLE kit.
Reach out to AVID Medical for specific instructions on handling affected kits.
Yes, metal flakes could enter surgical sites causing reactions or infections.
Check the model number and lot numbers; contact AVID Medical for next steps.
Affected kits have model LANC015-34 and lot numbers 1590497 or 1601534.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0406-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-0406-2025 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.
