# FDA recall Z-0780-2020

> **Stryker GmbH** · Class II · device recall initiated 2019-12-05.

## 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.

## Distribution

Worldwide distribution - US Nationwide distribution and countries of Switzerland, France, Spain, United Kingdom, Italy, Sweden, Netherlands, Australia.

## Key facts

- **Recall number:** Z-0780-2020
- **Recalling firm:** Stryker GmbH
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-05
- **Report date:** 2020-01-15
- **Termination date:** 2020-10-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Selzach, N/A, Switzerland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0780-2020

## Citation

> AI Analytics. FDA recall Z-0780-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0780-2020. Source: US FDA. Licensed CC0.

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