Synthes Battery Power Line II Oscillator Model 530 — Class II medical device recall Z-2345-2015
Terminated recall by The Anspach Effort, Inc., reported 2015-08-12, distributed in AR, LA, OH, WA. Saw head separated from the drive unit or began to come loose.
| Recall number | Z-2345-2015 |
|---|---|
| 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 | 2015-07-01 |
| Classified | 2015-08-05 |
| Reported by FDA | 2015-08-12 |
| Terminated | 2016-12-14 |
| Distributed | AR, LA, OH, WA |
| Countries outside the US | CH, CN, FR, GB, IT, RU, ZA |
| Serial numbers | 100020, 100026, 100039, 100055, 100063, 100065, 100067, 100069, 100076, 100248, 100254, 100257, 100263, 100265, 100269, 100270, 100293, 100296, 100307, 100313, 100315, 100339, 100340, 100371, 100372 |
| Model numbers | 530.710 |
Product
Synthes Battery Power Line II Oscillator Model 530.710, orthopedic surgical power tool.
Reason for recall
Saw head separated from the drive unit or began to come loose.
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-2345-2015. 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.