Avanos Medical recalls CORFLO Safety PEG Kit model 30-4320 due to contaminated lidocaine hydrochloride injection in sterile kits. Affected units have 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 recalls CORFLO Safety PEG Kit model 30-4320 because it contains lidocaine hydrochloride injection that was previously recalled for quality issues. This could pose a contamination risk to patients using the kit.
The lidocaine hydrochloride injection in the kit was previously recalled for quality issues. This means the injection may be contaminated, potentially causing harm to patients during medical procedures.
Healthcare professionals and patients using the CORFLO Safety PEG Kit model 30-4320 with lot numbers 30365226 or 30382750 are affected. Those using the kit for medical procedures are most at risk.
Check for the model number 30-4320 on the kit. Affected units have UDI-DI code 10350770007585 and lot numbers 30365226 or 30382750.
Look for model number 30-4320, UDI-DI code 10350770007585, and lot numbers 30365226 or 30382750 on the kit.
The lidocaine hydrochloride injection in the kit was previously recalled for quality issues, which could lead to contamination.
Check for model number 30-4320, UDI-DI code 10350770007585, and lot numbers 30365226 or 30382750.
The recall record does not specify a remedy, so contact Avanos Medical for guidance.
We’ve drafted a message you can send CORFLO to request your refund or repair — edit it as you like.
Subject: Recall Z-2333-2026 — CORFLO CORFLO Hello, I own a CORFLO that is covered by recall Z-2333-2026 from CORFLO. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.