Medical device recalls Moderate risk

The Anspach Effort, Inc. recalls Battery Power Line II Battery Oscillator, DePuy Synthes Power Tools, The Anspach Effort Inc.

Recall date
November 25, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2126-2016
FDA classification
Class II
Brand / firm
The Anspach Effort, Inc.
Sold / distributed
US Distribution to the state of : VA and Internationally to: Thailand and UK

Why it was recalled

Has the incorrect operating directions on the mode switch ring, i.e. its is labeled "FWD, LOCK, REV" instead of "ON, LOCK, ON".

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

What was recalled

Battery Power Line II Battery Oscillator, DePuy Synthes Power Tools, The Anspach Effort Inc.

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