Recall Z-1994-2016— The Anspach Effort, Inc.
Class II · Terminated
Class II FDA medical device recall by The Anspach Effort, Inc., initiated 2016-01-15, terminated 2016-12-14. FDA's recall record names no specific 510(k) clearance for this event. Product: Universal Battery Charger II (UBC II). Reason: The device is reported to enter safe mode and is no longer able to charge batteries..
- Recalling firm
- The Anspach Effort, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-01-15
- Terminated
- 2016-12-14
- Firm location
- Palm Beach Gardens, FL, United States
Product description
Universal Battery Charger II (UBC II)
Reason for recall
The device is reported to enter safe mode and is no longer able to charge batteries.
Data sourced from openFDA. This site is unofficial and independent of the FDA.