Class II — The Anspach Effort, Inc.
| Recalling firm | THE ANSPACH EFFORT, INC. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Saw head separated from the drive unit or began to come loose. |
| Product | Synthes Battery Power Line II Oscillator Model 530.710, orthopedic surgical power tool. |
| Quantity | 360 handpieces (Currently there are 9 affected units remaining in the US and 17 units OUS all others were reworked) |
| Distribution | Worldwide Distribution - US Distribution to the states of : AR, LA, OH, and WA., and the countries of : China, France, Italy, Russia, South Africa, Switzerland, and United Kingdom. |
| Initiated | 2015-07-01 |
| Classified | 2015-08-05 |
| Terminated | 2016-12-14 |
| Recall number | Z-2345-2015 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — The Anspach Effort, Inc. (Z-2345-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/71659/
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