FDA Device recall Z-0780-2020
Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and is used to support insertion and withdrawal of…
- FDA Device
- Class II
- terminated
- Published 2020-01-15
On 2020-01-15 the FDA classified a Class II recall of Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and is used to support insertion and withdrawal of… by Stryker, citing 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 rem….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0780-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-05 |
| Published | 2020-01-15 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Stryker |
| Distribution | US |
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
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.
Identifiers
| code_info | All lots UDI: (01)07613327350210 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0780-2020%22
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