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 | Terminated |
| Reason | The firm received complaints that the product is shorter in length than indicated on the label. |
| Product | AMT G-Jet® Low-Profile Transgastric-Jejunal Feeding Device 14F 1.5cm 45cm SINGLE USE ONLY Rx ONLY STERILE. For use in patients who cannot absorb adequate nutrition through the stomach. |
| Quantity | 20 units |
| Distribution | Distributed in the states of AZ, CA, DE, IN, MI, NM, PA & VA. |
| Initiated | 2016-01-26 |
| Classified | 2016-04-14 |
| Terminated | 2016-10-27 |
| Recall number | Z-1497-2016 |
| 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-1497-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/73339/
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