Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Synthes Battery Power Line II Oscillator Model 530.710 Recalled by The Anspach Effort, Inc. Due to Saw head separated from the drive unit or...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact The Anspach Effort, Inc. directly.
Affected Products
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)
Why Was This Recalled?
Saw head separated from the drive unit or began to come loose.
Where Was This Sold?
This product was distributed to 4 states: AR, LA, OH, WA
About The Anspach Effort, Inc.
The Anspach Effort, Inc. has 261 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report