Z-1994-2016 Class II Terminated
FDA device recall Z-1994-2016 was initiated by The Anspach Effort, Inc. on Jan 15, 2016 and is designated Class II. Reason for recall: The device is reported to enter safe mode and is no longer able to charge batteries. The recall status is terminated (terminated Dec 14, 2016). Affected quantity: 1,992.
Recall Details
- Product Type
- Devices
- Report Date
- Jun 22, 2016
- Initiation Date
- Jan 15, 2016
- Termination Date
- Dec 14, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,992
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.
Distribution Pattern
USA Distribution to the states of : AR, AZ, CA, CO, FL, IL, IN, LA, MA, MD, MI, MO, NC, NE, NJ, NM, NY, OK, OR, PA, SC, TN, TX, VA, WA, WI and Hawaii
Code Information
Part # 05.001.204 Serial #'s 10615 thru 12616
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1994-2016
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026