Avanos Medical recalls CORFLO Safety PEG Kit model 30-5320 due to contaminated 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 CORFLO Safety PEG Kits with model number 30-5320 because they contain lidocaine hydrochloride injection that was previously recalled for quality issues. This could lead to contamination risks if used in medical procedures.
The lidocaine hydrochloride injection in these kits was previously recalled for quality issues. This means the injection may not meet sterile standards, potentially causing contamination during medical procedures.
Healthcare professionals using CORFLO Safety PEG Kits with model 30-5320 are likely affected. Patients receiving procedures using these kits may be at risk if the contaminated lidocaine is administered.
Check for model number 30-5320 on the kit. Look for UDI-DI code 10350770007554 and lot numbers 30365227, 30368642, 30374529, 30376099, 30380696, or 30387248.
Verify the model number and lot numbers listed in the recall notice to confirm if your kit is affected.
The lidocaine hydrochloride injection in these kits was previously recalled for quality issues, meaning it may not meet sterile standards.
The recall notice does not specify a remedy, so check the kit details to see if it matches the affected model and lot numbers.
Look for model number 30-5320, UDI-DI code 10350770007554, and lot numbers 30365227, 30368642, 30374529, 30376099, 30380696, or 30387248.
We’ve drafted a message you can send CORFLO to request your refund or repair — edit it as you like.
Subject: Recall Z-2334-2026 — CORFLO CORFLO Hello, I own a CORFLO that is covered by recall Z-2334-2026 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.
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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.
