FDA recall record

The Anspach Effort Battery Power Line II Battery Oscillator, DePuy Synthes Power Tools, The recall — FDA Z-2126-2016

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

Class IIclassification
Z-2126-2016official record ID
Jul 13, 2016report date

Recall record at a glance

Official recordZ-2126-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmThe Anspach Effort, Inc.
Report dateJul 13, 2016
Recall initiation dateNov 25, 2015
Quantity20 hand pieces
LocationPalm Beach Gardens, FL, United States

Official product description

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

Why the product 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".

Distribution information

US Distribution to the state of : VA and Internationally to: Thailand and UK

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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