Battery Power Line II Battery Oscillator — Class II medical device recall Z-2126-2016
Terminated recall by The Anspach Effort, Inc., reported 2016-07-13. Has the incorrect operating directions on the mode switch ring, i.e. its is labeled "FWD, LOCK, REV" instead o
| Recall number | Z-2126-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Anspach Effort, Inc., Palm Beach Gardens, FL, United States |
| Recall initiated | 2015-11-25 |
| Classified | 2016-07-05 |
| Reported by FDA | 2016-07-13 |
| Terminated | 2018-11-14 |
| Countries outside the US | GB, TH |
| Quantity | 20 hand |
| Reason classes | labeling |
| Serial numbers | 101066, 101067, 101068, 101069, 101070, 101071, 101072, 101073, 101074, 101075, 101076, 101077, 101078, 101079, 101081, 101082, 101083, 101084, 101085, 1011080 |
| Model numbers | 530.710 |
Product
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".
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2126-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.