# FDA recall Z-2884-2018

> **Stryker GmbH** · Class II · device recall initiated 2018-06-27.

## Product

Stryker T2 ANKLE ARTHRODESIS NAIL RIGHT 10MMX200MM Item Number: 1819-1020S  T2 ANKLE ARTHRODESIS NAIL RIGHT 12MMX200MM 1819-1220S  T2 LONG PROXIMAL HUMERAL NAIL LEFT 240mm1832-2824S  T2 LONG PROXIMAL HUMERAL NAIL LEFT 280mm 1832-2828S  T2 LONG PROXIMAL HUMERAL NAIL RIGHT 260mm 1832-3826S  T2 Ankle Arthrd Nail lft 1818-1115S

## Reason for recall

Incomplete seal on the Tyvek lid  may compromise the sterility of the device

## Distribution

US distribution to KY

## Key facts

- **Recall number:** Z-2884-2018
- **Recalling firm:** Stryker GmbH
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-06-27
- **Report date:** 2018-08-29
- **Termination date:** 2020-04-13

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2884-2018

## Citation

> AI Analytics. FDA recall Z-2884-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-2884-2018. Source: US FDA. Licensed CC0.

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