Class II — Applied Medical Technology Inc
| Recalling firm | APPLIED MEDICAL TECHNOLOGY, INC. |
|---|---|
| Registered facility | APPLIED MEDICAL TECHNOLOGY, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Completed |
| Reason | 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. |
| Product | AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222 |
| Quantity | 100 |
| Distribution | US Distribution to states of: CA, CT, FL, GA, IL, MA, MD, MO, NC, NJ, NY, OH, OK, PA, SC, TX, VA, WA |
| Initiated | 2024-11-26 |
| Classified | 2025-01-07 |
| Recall number | Z-0819-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Applied Medical Technology Inc (Z-0819-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/95881/
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