Universal Battery Charger II — Class II medical device recall Z-1994-2016
Terminated recall by The Anspach Effort, Inc., reported 2016-06-22, distributed in AR, AZ, CA, CO, FL, HI, IL, IN…. The device is reported to enter safe mode and is no longer able to charge batteries.
| Recall number | Z-1994-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Anspach Effort, Inc., Palm Beach Gardens, FL, United States |
| Recall initiated | 2016-01-15 |
| Classified | 2016-06-15 |
| Reported by FDA | 2016-06-22 |
| Terminated | 2016-12-14 |
| Distributed | AR, AZ, CA, CO, FL, HI, IL, IN, LA, MA, MD, MI, MO, NC, NE, NJ, NM, NY, OK, OR, PA, SC, TN, TX, VA, WA, WI |
| Quantity | 1,992 |
| Serial numbers | 10615 |
| Model numbers | 05.001.204 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1994-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.