Avanos Medical recalls pediatric neonatal feeding tubes with anti-IV connector due to risk of male AIV adaptor detaching from Y-connector. Affected units have specific product codes and lot numbers.
Detachment of the Male AIV Adaptor from the Y-Connector.
Avanos Medical is recalling pediatric neonatal feeding tubes that may detach the male AIV adaptor from the Y-:connector. This could cause injury to infants during medical procedures.
The male AIV adaptor can detach from the Y-connector during use, potentially causing the feeding tube to disconnect from the infant's feeding system. This could lead to the infant receiving improper nutrition or causing injury during medical procedures.
Infants receiving neonatal care using the recalled feeding tubes. Healthcare providers and caregivers who handle these tubes are most at risk.
Check for product code 20-1225AIV and lot number 0002983985 on the tube packaging or label. The product was sold to healthcare facilities and neonatal care providers.
Inspect the male AIV adaptor for signs of detachment from the Y-connector on the feeding tube.
The recall indicates a risk of detachment, so it is not safe to use without checking for the issue.
Look for product code 20-1225AIV and lot number 0002983985 on the tube packaging or label.
The recall does not specify a remedy, so contact Avanos Medical for guidance.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0540-2021 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-0540-2021 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.