Stryker T2 Alpha Delta Strike Plate IMN Instruments — Class II medical device recall Z-0780-2020
Terminated recall by Stryker GmbH, reported 2020-01-15, distributed nationwide. Instrument can break at the level of the thread when being exposed to high forces during nail implantation or
| Recall number | Z-0780-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker GmbH, Selzach, N/A, Switzerland |
| Recall initiated | 2019-12-05 |
| Classified | 2020-01-07 |
| Reported by FDA | 2020-01-15 |
| Terminated | 2020-10-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CH, ES, FR, GB, IT, NL, SE |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 07613327350210 |
| Model numbers | 2351-0050 |
Product
Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and is used to support insertion and withdrawal of nails through the Targeting Device Catalog Number: 2351-0050
Reason for recall
Instrument can break at the level of the thread when being exposed to high forces during nail implantation or removal which can lead to complications during nail insertion and removal.
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-0780-2020. 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.