RecallRadar

FDA Device recall Z-2126-2016

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

On 2016-07-13 the FDA classified a Class II recall of Battery Power Line II Battery Oscillator, DePuy Synthes Power Tools, The Anspach Effort Inc by The Anspach Effort, citing has the incorrect operating directions on the mode switch ring, i.e. its is labeled "FWD, LOCK, REV" instead of "ON, LOCK, ON".

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2126-2016
ClassificationClass II
Statusterminated
Initiated2015-11-25
Published2016-07-13
Last updated2026-09-13 11:54 UTC
CompanyThe Anspach Effort
DistributionVA

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".

Identifiers

code_info
Part Number 530.710, Serial Numbers 101066, 101067, 101068, 101069, 101070, 101071, 101072, 101073, 101074, 101075, 101…Part Number 530.710, Serial Numbers 101066, 101067, 101068, 101069, 101070, 101071, 101072, 101073, 101074, 101075, 101076, 101077, 101078, 101079, 1011080, 101081, 101082, 101083, 101084, 101085

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2126-2016%22

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