Avanos Medical recalls 24 Fr PULL PEG kits with lidocaine hydrochloride injection due to quality issues in sterile kits. Affected units include specific model numbers and lot numbers.
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Avanos Medical is recalling their 24 Fr PULL PEG kits because they contain lidocaine hydrochloride injection that was found to have quality issues. This could lead to contamination or infection risks if used improperly.
The lidocaine hydrochloride injection was included in sterile kits that were supposed to be free of such substances. This could lead to contamination or infection if the kits are used without proper sterilization.
Healthcare professionals who use the PEG kits for medical procedures may be affected. Patients receiving these kits are at risk if the kits are contaminated.
Check for model number 7180-24 and lot numbers 30371316, 30377829, or 80403341 on the kit packaging. The product is sold under the brand Avanos Medical.
Verify the model number and lot numbers on the kit packaging to confirm if it is affected.
The recall states that lidocaine hydrochloride injection was included in sterile kits, which could pose a contamination risk. Affected units should not be used until the remedy is applied.
Check the model number and lot numbers on the kit packaging. If it matches the affected units, contact Avanos Medical for further instructions.
Look for model number 7180-24 and lot numbers 30371316, 30377829, or 80403341 on the packaging.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2346-2026 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-2346-2026 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.
