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Stryker GmbH recalls Endotrac EPF/EGR Hook Blade, Catalog Number 3055-1 The EPF system is designed for the treatment of plantar fasciosis
Recalled September 4, 2019 · FDA recall Z-2418-2019 · Stryker
Hazard
The seal integrity of the sterile bag containing the kits may be compromised. · FDA Class II
Units
2248
Sold at
US Nationwide Distribution
Description
The seal integrity of the sterile bag containing the kits may be compromised.
Product
Endotrac EPF/EGR Hook Blade, Catalog Number 3055-1 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 →