AMT Initial Placement Dilator Set — Class II medical device recall Z-2238-2024
Completed recall by Applied Medical Technology Inc, reported 2024-07-10, distributed nationwide. Devices were labelled with the incorrect guidewire labelling.
| Recall number | Z-2238-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Applied Medical Technology Inc, Brecksville, OH, United States |
| Recall initiated | 2024-05-14 |
| Classified | 2024-06-28 |
| Reported by FDA | 2024-07-10 |
| Distributed | Nationwide (US) |
| Quantity | 74 units |
| UPC / GTIN / UDI-DI | 00842071131876 |
| Lot numbers | 231218-242 |
| Expiration dates | 2026-11-01 |
Product
AMT Initial Placement Dilator Set. Used to place gastrostomy devices.
Reason for recall
Devices were labelled with the incorrect guidewire labelling.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2238-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.