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The Anspach Effort, Inc. recalls Synthes Battery Power Line II Oscillator Model 530.710, orthopedic surgical power tool.
Recalled August 12, 2015 · FDA recall Z-2345-2015 · The Anspach Effort
Hazard
Saw head separated from the drive unit or began to come loose. · FDA Class II
Units
360 handpieces (Currently there are 9 affected units remaining in the US and 17 units OUS all others were reworked)
Sold at
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.
Description
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.
Manufacturer(s)
The Anspach Effort, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →