The Anspach Effort, Inc. recalls Synthes Battery Power Line II Oscillator Model 530.710, orthopedic surgical power tool.
- Recall date
- July 1, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2345-2015
- FDA classification
- Class II
- Brand / firm
- The Anspach Effort, Inc.
- Sold / distributed
- 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.
Why it was recalled
Saw head separated from the drive unit or began to come loose.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Synthes Battery Power Line II Oscillator Model 530.710, orthopedic surgical power tool.
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