Medical device recalls Moderate risk

The Anspach Effort, Inc. recalls Universal Battery Charger II (UBC II)

Recall date
January 15, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1994-2016
FDA classification
Class II
Brand / firm
The Anspach Effort, Inc.
Sold / distributed
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

Why it was recalled

The device is reported to enter safe mode and is no longer able to charge batteries.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Universal Battery Charger II (UBC II)

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