Avanos Medical recalls CORFLO Safety PEG Kit with ENFit Connector (model 50-5320) due to potential contamination from lidocaine hydrochloride injection 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 50-5320) because sterile kits may contain lidocaine hydrochloride injection from a supplier recall. This contamination could lead to infections or other health risks if used improperly.
The sterile kits may contain lidocaine hydrochloride injection, which was previously recalled by the supplier for quality issues. This contamination could lead to infections or other health risks if the kit is used without proper sterilization.
Healthcare professionals using the CORFLO Safety PEG Kit with ENFit Connector for medical procedures are most at risk. Patients receiving treatments with this kit could be affected if the contaminated kit is used.
Check for the model number 50-5320 on the kit. Look for UDI-DI code 10350770007516 and lot numbers 30365231, 30371022, 30373824, 30378385, 30383807, or 30385321.
Identify the model number (50-5320) and UDI-DI code (10350770007516) on the kit to confirm if it is affected.
The sterile kits may contain lidocaine hydrochloride injection from a supplier recall for quality issues, which could lead to contamination.
The recall record does not specify a remedy, so check the kit details to confirm if it is affected and contact Avanos Medical for further instructions.
Look for the model number 50-5320, UDI-DI code 10350770007516, and lot numbers 30365231, 30371022, 30373824, 30378385, 30383807, or 30385321.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2338-2026 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2338-2026 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.
