Applied Medical Technology recalls AMT Mini Enteral Extension Set model E6-1222 due to ENFit connectors that may not fit with non-ENFit devices, risking incorrect feeding tube connections.
The extension sets subject to this recall have ENFit connections, although they should have non- ENFit connections. ENFit connectors will only fit with other ENFit-compatible devices, and will not fit with non-ENFit connectors.
Applied Medical Technology is recalling their AMT Mini Enteral Extension Set (model E6-1:222) because it has ENFit connectors instead of the required non-ENFit connectors. This could lead to incorrect feeding tube connections if used with non-ENFit devices, potentially causing injury.
ENFit connectors only fit with other ENFit-compatible devices and will not fit with non-ENFit connectors. This mismatch could cause incorrect feeding tube connections, potentially leading to injury if the tube is not properly secured.
Patients using enteral feeding tubes and caregivers who handle the feeding equipment are most at risk. The recall affects specific model numbers sold between 2024 and 2027.
Check for the model number E6-1222 on the product. The product was sold between 2024 and 2027 with an expiration date of April 2027.
Look for the model number E6-1222 on the extension set.
The extension sets have ENFit connectors instead of the required non-ENFit connectors, which may not fit with non-ENFit devices and could cause incorrect feeding tube connections.
Check for the model number E6-1222 on the product. The product was sold between 2024 and 2027 with an expiration date of April 2027.
The recall does not specify a remedy, so contact Applied Medical Technology for guidance.
We’ve drafted a message you can send Applied Medical Technology to request your refund or repair — edit it as you like.
Subject: Recall Z-0819-2025 — Applied Medical Technology Applied Medical Technology Hello, I own a Applied Medical Technology that is covered by recall Z-0819-2025 from Applied Medical Technology. 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.
