FDA Device recall Z-2126-2016
Battery Power Line II Battery Oscillator, DePuy Synthes Power Tools, The Anspach Effort Inc
- FDA Device
- Class II
- terminated
- Published 2016-07-13
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
| Agency | FDA Device |
|---|---|
| Recall number | Z-2126-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-11-25 |
| Published | 2016-07-13 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | The Anspach Effort |
| Distribution | VA |
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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