Avanos Medical recalls CORFLO Safety PEG Kit with ENFit Connector (model 50-6312) due to potential lidocaine hydrochloride contamination 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 50-6312) because sterile kits may contain lidocaine hydrochloride injection from a supplier recall. This contamination could affect medical safety during use.
The sterile kits may contain lidocaine hydrochloride injection, which was previously recalled by the supplier for quality issues. This contamination could compromise the sterility of the medical kit during procedures.
Healthcare professionals using the CORFLO Safety PEG Kit with ENFit Connector for medical procedures are most at risk. Patients receiving treatments with this kit may be affected if contaminated.
Check for model number 50-6312 on the kit. Affected units have UDI-DI 10350770007523 and lot numbers 30365232, 30367019, or 30380107.
Identify the model number (50-6312) and UDI-DI code (10350770007523) to confirm if your kit is affected.
The sterile kits may contain lidocaine hydrochloride injection from a supplier recall for quality issues.
Check the model number and UDI-DI code to see if your kit is affected; no specific action is required if it's not listed.
The contamination could compromise medical sterility during procedures, but the recall is for quality issues, not immediate harm.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2339-2026 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2339-2026 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.
