Avanos Medical recalls PEG kits with ENFit connectors due to lidocaine hydrochloride injection 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 PEG kits with EN:Fit connectors because they contain lidocaine hydrochloride injections that were found to have quality issues. This could lead to contamination risks during medical procedures.
The lidocaine hydrochloride injections were included in sterile kits without proper quality checks. This could lead to contamination or improper medication delivery during medical procedures.
Healthcare professionals using these kits for medical procedures are most at risk. Patients receiving treatments with the recalled kits may also be affected.
Check for model number 8170-24 and lot numbers 30371847, 30374834, 30378748, or 30380347 on the kit packaging. The product includes ENFit connectors and is labeled as a 24 Fr PUSH OTW PEG kit.
Verify the model number and lot numbers on the kit packaging to determine if it is affected.
The lidocaine hydrochloride injections were included in sterile kits without proper quality checks, leading to potential contamination risks.
Check the model number and lot numbers on the packaging to see if it is affected. If it is, contact Avanos Medical for further instructions.
The recall is due to quality issues with lidocaine hydrochloride injections, which could lead to contamination during medical procedures.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2349-2026 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2349-2026 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.
