Avanos Medical recalls CORFLO Safety PEG Kit with ENFit Connector (model 50-6316) due to sterile kits containing lidocaine hydrochloride injection from a supplier with quality issues. Affected units have specific 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 their CORFLO Safety PEG Kit with ENFit Connector (model 50-6316) because it may contain lidocaine hydrochloride injection from a supplier with quality issues. This could pose a risk of contamination in sterile feeding kits.
The sterile feeding kits may contain lidocaine hydrochloride injection that was recalled by the supplier due to quality issues. This could lead to contamination of the sterile kit, potentially causing infection or other health risks if used.
People using the CORFLO Safety PEG Kit with ENFit Connector for feeding tube setups are likely affected. Those with the specific lot numbers listed in the recall are at higher risk.
Check for the model number 50-6316 on the CORFLO Safety PEG Kit with ENFit Connector. Affected units have lot numbers 30365233, 30367015, 30372821, or 30378386.
Look for lot numbers 30365233, 30367015, 30372821, or 30378386 on the kit.
The sterile kits may contain lidocaine hydrochloride injection from a supplier with quality issues, which could lead to contamination.
Check the lot numbers on the kit. If it matches the listed numbers, contact Avanos Medical for instructions.
The recall is for potential contamination, but the official notice does not specify a risk of serious injury.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2340-2026 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2340-2026 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.
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.
