Avanos Medical recalls PEG kits with ENFit connectors due to potential lidocaine contamination in sterile kits. Affected units include specific model numbers and lot dates. Consumers should contact the manufacturer for details.
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical is recalling PEG kits with ENFit connectors because they may contain lidocaine hydrochloride injection, which was part of a supplier recall for quality issues. This contamination could affect the sterility of the kits and pose risks during medical procedures.
Lidocaine hydrochloride injection, which was recalled by the supplier for quality issues, was included in the sterile kits. This contamination could compromise the sterility of the kits and potentially lead to infections during medical procedures.
Healthcare professionals using the PEG kits for medical procedures are most at risk. Patients receiving these kits may also be affected if the contamination occurs.
Check for model number 8180-14 and lot numbers 30371318, 30375469, or 30383056 on the kit packaging. The kits have ENFit connectors and are labeled as '14 Fr PULL'.
Reach out to Avanos Medical directly for specific instructions on how to verify if your kit is affected and what to do next.
The kits may contain lidocaine hydrochloride injection, which was part of a supplier recall for quality issues.
Check for model number 8180-14 and lot numbers 30371318, 30375469, or 30383056 on the kit packaging.
Contact Avanos Medical directly for specific instructions on how to verify and address the issue.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2350-2026 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2350-2026 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.
