# FDA recall Z-2422-2019

> **Stryker GmbH** · Class II · device recall initiated 2019-07-25.

## Product

Endotrac EPF/EGR Triangle Blade, Angled, Catalog Number 3054A-1     The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.

## Reason for recall

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

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-2422-2019
- **Recalling firm:** Stryker GmbH
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-25
- **Report date:** 2019-09-04
- **Termination date:** 2020-09-24

- **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-2422-2019

## Citation

> AI Analytics. FDA recall Z-2422-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2422-2019. Source: US FDA. Licensed CC0.

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