AVID Medical recalls ENT packs with model JACK421-04 due to potential open header bag seals that could compromise sterility. Affected units were sold from 2021 to 2027.
Potential for open header bag seals, compromising sterility.
AVID Medical is recalling ENT packs with model number JACK421-04 because the packaging might not stay sealed properly, risking contamination. This could affect surgical procedures if the packs are used without proper sterility.
The header bag seals on these packs might open, which could allow contamination. This is a sterility risk in medical settings, but it doesn't cause injury directly.
Patients and medical professionals who use these ENT packs for procedures. The risk is low as the issue is about packaging integrity, not immediate harm.
Check for model number JACK421-04 on the pack. Units were sold from 2021 to 2027 with lot number 1647218 and expiration date 7/17/2027.
Look for open or damaged header bag seals on the pack.
The recall is due to potential packaging issues that could compromise sterility, but the product itself is not unsafe if used properly.
Check for model number JACK421-04, lot number 1647218, and expiration date 7/17/2027.
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-2530-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2530-2025 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.
