Medical device recalls Moderate risk

Smith & Nephew, Inc. recalls Smith & Nephew Dyonics Saw Blade, Short, Narrow, Product Number 3704

Recall date
February 2, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1242-2017
FDA classification
Class II
Brand / firm
Smith & Nephew, Inc.
Sold / distributed
Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela

Why it was recalled

The single use devices are provided sterile and do not have an expiration date on the label.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Smith & Nephew Dyonics Saw Blade, Short, Narrow, Product Number 3704

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