Use cautionMedical device recall · FDA · Published November 26, 2024
Applied Medical Technology recalls AMT Mini Enteral Extension Set with ENFit connection
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. Read more at govinfonow.com/recall/53388-applied-medical-technology-recalls-amt-mini-enteral-extension-set-with.
“Applied Medical Technology recalls AMT Mini Enteral Extension Set with ENFit connection.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/53388-applied-medical-technology-recalls-amt-mini-enteral-extension-set-with. Based on FDA recall #Z-0819-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0819-2025%22&limit=1).
The FDA announced on November 26, 2024, that Applied Medical Technology Inc is recalling the AMT Mini Enteral Extension Set due to incorrect connector types. The company said owners should stop using the product and contact the firm for a refund.
How to tell if you have it
Brand: Applied Medical Technology
Product: AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port
Model/Catalog Number: E6-1222
UPC: 00842071107086
Lot Code: 240424-628
Expiration Date: 2027-04-01
The hazard
The extension sets have ENFit connections instead of the required non-ENFit connections. This incompatibility means the connectors will not fit with non-ENFit devices, according to the FDA.
Context
GovInfoNow's records show Applied Medical Technology Inc has had four other recalls since November 10, 2020. Other recent recalls of similar products include NutraGlide Nasal Feeding Tube Recall (2025-10-06), NutraGlide Nasal Feeding Tubes Recall (2025-08-12), and Applied Medical Technology AMT Initial Placement Dilator Set Recall (2024-05-14). Other recent recalls of similar products include Medline ENFIT G-Tube Connectors May Leak (2026-02-13), Medline ENFIT G-TUBE Connector Recall (2026-02-13), and Medela ENFit ExSet Strl 60 2.0ml PV 1ct EN (2026-06-05).
How to tell if you have this one
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.
Brand
Applied Medical Technology
Product
AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Model
Look for the model number E6-1222 on the extension set.
Where it went and when
Where it was distributed
Distributed in 18 states.
Listed by the agency
Not listed
FDA distribution: “US Distribution to states of: CA, CT, FL, GA, IL, MA, MD, MO, NC, NJ, NY, OH, OK, PA, SC, TX, VA, WA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Connecticut, Florida, Georgia, Illinois, Maryland, Massachusetts, Missouri, New Jersey, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, South Carolina, Texas, Virginia, Washington.
Recall timeline
FDA published this recall 50 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-0819-2025 (November 26, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0819-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.