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Stryker GmbH recalls Endotrig ETF Hook Blade, Catalog Number 1052-1 The EPF system is designed for the treatment of plantar fasciosis. The
Recalled September 4, 2019 · FDA recall Z-2412-2019 · Stryker
Hazard
The seal integrity of the sterile bag containing the kits may be compromised. · FDA Class II
Units
35
Sold at
US Nationwide Distribution
Description
The seal integrity of the sterile bag containing the kits may be compromised.
Product
Endotrig ETF Hook Blade, Catalog Number 1052-1 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 →