Avanos Medical recalls 20 Fr PULL PEG kits with lidocaine hydrochloride injection due to quality issues in sterile kits. Affected units include specific model numbers and lot numbers.
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical is recalling their 20 Fr PULL PEG kits because they contain lidocaine hydrochloride injection that was found to have quality issues. This could lead to contamination risks if the kits are used for medical procedures.
The lidocaine hydrochloride injection was included in sterile kits that were supposed to be free of such substances. This could lead to contamination risks during medical procedures if the injection is not properly sterilized.
Healthcare professionals using the PEG kits for medical procedures are most at risk. Patients receiving these kits may be affected if the kits are used improperly.
Check for model number 7180-20 and lot numbers 30371313, 30371314, 30373295, 30373296, 30374832, 30378735, or 80403340 on the kit packaging.
Look for model number 7180-20 and lot numbers listed in the recall notice.
The model number is 7180-20.
Lot numbers 30371313, 30371314, 30373295, 30373296, 30374832, 30378735, and 80403340 are affected.
The recall notice does not specify a remedy.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2345-2026 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2345-2026 from Avanos 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.
