Recall Z-2345-2015— The Anspach Effort, Inc.
Class II · Terminated
Class II FDA medical device recall by The Anspach Effort, Inc., initiated 2015-07-01, terminated 2016-12-14. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- The Anspach Effort, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-07-01
- Terminated
- 2016-12-14
- Firm location
- Palm Beach Gardens, FL, United States
Product description
Synthes Battery Power Line II Oscillator Model 530.710, orthopedic surgical power tool.
Reason for recall
Saw head separated from the drive unit or began to come loose.
Data sourced from openFDA. This site is unofficial and independent of the FDA.