Avanos Medical recalls CORFLO Safety PEG Kit model 30-6316 due to contaminated lidocaine hydrochloride injection in sterile kits. Affected units include specific lot numbers and model.
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical is recalling its CORF: Safety PEG Kit model 30-6316 because it contains lidocaine hydrochloride injection that was previously recalled for quality issues. This poses a risk of contamination in sterile medical kits.
The kit includes lidocaine hydrochloride injection that was previously recalled by the supplier for quality issues. This means the injection could be contaminated, potentially causing adverse effects in medical procedures.
Healthcare professionals using the CORFLO Safety PEG Kit for medical procedures may be affected. Patients receiving injections from this kit could be at risk if the lidocaine is contaminated.
Check for model number 30-6316 on the kit. Affected units have lot numbers 30365229 and 30376100 or UDI-DI 10350770007561.
Verify the model number and lot numbers to confirm if your kit is affected.
The recall states the lidocaine hydrochloride injection was previously recalled for quality issues, so it may be contaminated. Do not use the kit until confirmed safe.
Check the model number and lot numbers to see if your kit is affected. If it is, stop using it and contact Avanos Medical for further instructions.
Look for model number 30-6316 with lot numbers 30365229 or 30376100, or UDI-DI 10350770007561.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2336-2026 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2336-2026 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.
