Avanos Medical recalls CORFLO Safety PEG Kit with ENFit Connector (model 50-4320) due to lidocaine hydrochloride injection quality issues in sterile kits. Affected units include specific lot numbers and UDI-DI codes.
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical is recalling its CORFLO Safety PEG Kit with ENFit Connector (model 50-4320) because lidocaine hydrochloride injections were included in sterile kits during manufacturing. This could lead to contamination risks if the kit is used for medical procedures.
Lidocaine hydrochloride injections were included in sterile kits during manufacturing, which could lead to contamination. This poses a risk of improper medication delivery if the kit is used for medical procedures.
Healthcare professionals using the CORFLO Safety PEG Kit with ENFit Connector for medical procedures are most at risk. Patients receiving injections through this kit could be affected if the lidocaine is contaminated.
Check for the model number 50-4320 on the kit. Look for UDI-DI code 10350770007578 and lot numbers 30365230, 30367013, or 30373825.
Verify the model number (50-4320), UDI-DI code (10350770007578), and lot numbers (30365230, 30367013, 30373825) to confirm if your kit is affected.
The recall is due to lidocaine hydrochloride injections being included in sterile kits during manufacturing, which could lead to contamination risks.
Check for the model number 50-4320, UDI-DI code 10350770007578, and lot numbers 30365230, 30367013, or 30373825.
The recall record does not specify a remedy, so contact Avanos Medical directly for guidance.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2337-2026 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2337-2026 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.
