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 | Devices were labelled with the incorrect guidewire labelling. |
| Product | AMT Initial Placement Dilator Set. Used to place gastrostomy devices. |
| Quantity | 74 units |
| Distribution | US Nationwide distribution in the states of GA, IL, IN, LA, NC, NE, SC, TN, TX, UT, VA, WA, & WV. |
| Initiated | 2024-05-14 |
| Classified | 2024-06-28 |
| Recall number | Z-2238-2024 |
| 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-2238-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94702/
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