# FDA recall Z-1849-2019

> **Stryker GmbH** · Class II · device recall initiated 2019-04-30.

## Product

Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1

## Reason for recall

The seal integrity of the sterile bag containing the kits may be compromised.

## Distribution

The products were distributed US nationwide.

## Key facts

- **Recall number:** Z-1849-2019
- **Recalling firm:** Stryker GmbH
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-04-30
- **Report date:** 2019-06-26
- **Termination date:** 2020-09-18

- **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-1849-2019

## Citation

> AI Analytics. FDA recall Z-1849-2019. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1849-2019. Source: US FDA. Licensed CC0.

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