Recall of Avanos MIC-KEY Gastric-Jejunal Feeding Tube Kits with missing risk information in instructions. Affected models include non-ENFIT and ENFit connectors. No action required per official notice.
The IFU was missing some risk information requested by another country to be contained in the IFU pertaining to potential complications.
Avanos Medical is recalling certain MIC-KEY Gastric-Jejunal Feeding Tube Kits due to missing risk information in the instructions. This is a non-urgent recall with no action required by the manufacturer.
The recall is for missing risk information in the instructions that was requested by another country. This means users might not have the full safety details needed for proper use, but it does not indicate an immediate physical hazard.
Patients using these feeding tube kits for medical nutrition support. Healthcare providers who have the affected models may be at risk if they use the kits without updated instructions.
Check for product codes starting with 0270- or 8270- followed by the size (e.g., 14 Fr, 16 Fr) and the specific UDI-DI numbers listed in the recall notice. All lot numbers are affected.
Review the product code and UDI-DI numbers to confirm if your kit is affected. The recall includes specific models with non-ENFIT and ENFit connectors.
No action is required per the official recall notice. The manufacturer states the missing information does not pose an immediate hazard.
Affected models include MIC-KEY Gastric-Jejunal Feeding Tube Kits with product codes starting with 0270- or 8270- and specific UDI-DI numbers listed in the recall notice.
The recall is for missing risk information in the instructions, not an immediate physical hazard. No serious injury risk is described in the notice.
We’ve drafted a message you can send Avanos to request your refund or repair — edit it as you like.
Subject: Recall Z-2422-2024 — Avanos Avanos Hello, I own a Avanos that is covered by recall Z-2422-2024 from Avanos. 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.
