Avanos Medical recalls PEG kits with ENFit connectors that contain lidocaine hydrochloride injection due to quality issues in sterile kits. Affected kits may have non-sterile components.
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 that include lidocaine hydrochloride injection, which was found in sterile kits due to quality issues. This could lead to infections or other complications if used improperly.
The kits contain lidocaine hydrochloride injection that was not properly sterilized, which could lead to infections or other complications if used in medical procedures. This is a quality issue from the supplier, not a design flaw.
Healthcare professionals using the PEG kits for medical procedures are most at risk. Patients receiving these kits could also be affected if the lidocaine causes contamination.
Check for the model number 8170-20 on the kit. The lot numbers 30371324, 30374833, 30384889, and 80403350 are also associated with this recall.
Verify the model number and lot numbers listed in the recall notice to confirm if your kit is affected.
The kits contain lidocaine hydrochloride injection that was not properly sterilized, which could lead to infections or complications during medical procedures.
Check for the model number 8170-20 and lot numbers 30371324, 30374833, 30384889, or 80403350 on the kit.
The recall notice does not specify a remedy, so contact Avanos Medical directly for further instructions.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2348-2026 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2348-2026 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.
