Avanos Medical recalls PEG kits with ENFit connectors that contain lidocaine hydrochloride injection from a supplier with quality issues. These kits may have contaminated sterile components.
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical is recalling PEG kits with ENFit connectors that include lidocaine hydrochloride injection from a supplier with quality issues. This could mean the sterile kits are contaminated, posing a risk of infection or other complications during medical procedures.
The kits contain lidocaine hydrochloride injection that was part of a supplier recall for quality issues. This means the sterile components might be contaminated, increasing the risk of infection or other complications during medical procedures.
Healthcare providers using these specific PEG kits for medical procedures are most at risk. Patients receiving these kits may face infection or other complications due to contaminated components.
Check for model number 8180-20, lot numbers 20133232, 30371326, 30378749, 30378751, 30379686, 30383063, 30383057, 80403339, or 80403342 on the kit packaging.
Verify the model number and lot numbers listed in the recall notice to confirm if your kit is affected.
The kits contain lidocaine hydrochloride injection that was part of a supplier recall for quality issues, which may mean the sterile components are contaminated.
The recall notice 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 model number 8180-20 and lot numbers listed in the recall notice: 20133232, 30371326, 30378749, 30378751, 30379686, 30383063, 30383057, 80403339, or 80403342.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2351-2026 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2351-2026 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.
