Home / Recalls / Medical Devices
Smith & Nephew, Inc. recalls Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701
Recalled March 1, 2017 · FDA recall Z-1239-2017 · Smith & Nephew
Hazard
The single use devices are provided sterile and do not have an expiration date on the label. · FDA Class II
Units
2646
Sold at
Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela
Description
The single use devices are provided sterile and do not have an expiration date on the label.
Product
Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701
Manufacturer(s)
Smith & Nephew, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →