Stryker GmbH recalls Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed for the treatment of plantar fasciosis

Recalled September 4, 2019 · FDA recall Z-2416-2019 · Stryker

Hazard

The seal integrity of the sterile bag containing the kits may be compromised. · FDA Class II

Units

251

Sold at

US Nationwide Distribution

Description

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

Product

Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 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.

Manufacturer(s)

Stryker GmbH

Made in

Switzerland

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →