FDA Device recall Z-2345-2015
Synthes Battery Power Line II Oscillator Model 530.710, orthopedic surgical power tool
- FDA Device
- Class II
- terminated
- Published 2015-08-12
On 2015-08-12 the FDA classified a Class II recall of Synthes Battery Power Line II Oscillator Model 530.710, orthopedic surgical power tool by The Anspach Effort, citing saw head separated from the drive unit or began to come loose.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2345-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-01 |
| Published | 2015-08-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | The Anspach Effort |
| Distribution | AR, LA, OH, WA |
Product
Synthes Battery Power Line II Oscillator Model 530.710, orthopedic surgical power tool.
Reason
Saw head separated from the drive unit or began to come loose.
Identifiers
| code_info | Serial numbers: 100067, 100076, 100371, 100372, 100063, 100065, 100069, 100076, and 100055; Foreign: Item number 530.7…Serial numbers: 100067, 100076, 100371, 100372, 100063, 100065, 100069, 100076, and 100055; Foreign: Item number 530.710 Serial numbers: 100020, 100026, 100039, 100248, 100254, 100257, 100263, 100265, 100269, 100270, 100293, 100296, 100307, 100313, 100315, 100339, and 100340. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2345-2015%22
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