Avanos Medical recalls PEG kits with lidocaine hydrochloride injection due to quality issues in sterile kits. Affected kits have model 7170-24 and lot numbers 30370715, 30371329, 30375466.
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 that contain lidocaine hydrochloride injection, which was found to have quality issues. This could affect the safety of the sterile kits used for feeding tubes.
The lidocaine hydrochloride injection was included in sterile kits due to a supplier recall for quality issues. This could lead to contamination if the injection is not properly sterile, potentially causing infections or other complications.
Healthcare providers using the PEG kits for feeding tube procedures may be affected. Patients receiving these kits are at risk if the lidocaine hydrochloride injection is not properly sterile.
Check for model number 7170-24 and lot numbers 30370715, 30371329, or 30375466 on the kit packaging.
Look for model number 7170-24 and lot numbers 30370715, 30371329, or 30375466 on the kit packaging.
The lidocaine hydrochloride injection was included in sterile kits due to a supplier recall for quality issues.
Check the model number and lot numbers on the packaging to see if it is affected. If it is, contact Avanos Medical for further instructions.
The quality issues could lead to contamination, but the risk is low as the product is for medical use and the issue is related to a supplier's quality problems.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2343-2026 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2343-2026 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.
