AVID Medical recalls GS Endoscopy Packs (models NAMC421-10 to NAMC421-12) due to discoloration from resterilization. Affected kits may have visual issues during procedures.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
AVID Medical is recalling endoscopy packs that may have discoloration from improper resterilization. This could affect visualization during medical procedures, though it's not a safety hazard.
The visualization system in the packs was resterilized incorrectly, causing discoloration. This may lead to visual issues during endoscopic procedures, but it does not pose a safety risk.
Medical professionals using the recalled endoscopy packs for procedures. Those with the specific model numbers and lot numbers listed are most at risk.
Check for model numbers NAMC421-10, NAMC421-11, or NAMC421-12. Also look for lot numbers 1584375, 1588403, 1605341, 1615427, 1615428, 1627706, 1628153, 1628008, 1628009, 1628647, or 1632992.
Inspect the visualization system for discoloration before use.
The visualization system was inadvertently resterilized, causing discoloration in some kits.
No, this is a cosmetic issue that may affect visualization but does not pose a safety risk.
Check for model numbers NAMC421-10, NAMC421-11, or NAMC421-12 and lot numbers listed in the recall notice.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2249-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2249-2025 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.
