Recall Z-2126-2016— The Anspach Effort, Inc.

Name: FDA recall Z-2126-2016
Creator: U.S. Food and Drug Administration
Published: 2015-11-25

Class II · Terminated

Class II FDA medical device recall by The Anspach Effort, Inc., initiated 2015-11-25, terminated 2018-11-14. FDA's recall record names no specific 510(k) clearance for this event. Product: Battery Power Line II Battery Oscillator, DePuy Synthes Power Tools, The Anspach Effort Inc.. Reason: Has the incorrect operating directions on the mode switch ring, i.e. its is labeled "FWD, LOCK, REV" instead of "ON, LOCK, ON"..

Recalling firm: The Anspach Effort, Inc.
Classification: Class II
Status: Terminated
Initiated: 2015-11-25
Terminated: 2018-11-14
Firm location: Palm Beach Gardens, FL, United States

Product description

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

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.