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Cardiocommand Inc. recalls TAPSYSTEM Model 2A, REF 8002A
Recalled July 24, 2019 · FDA recall Z-1976-2019 · Cardiocommand
Hazard
There is a potential for an assembly error resulting in the battery wire being connected to the ON/OFF power switch incorrectly. · FDA Class III
Units
6 units
Sold at
United States - AR, NM, PA, TX, and WA.
Description
There is a potential for an assembly error resulting in the battery wire being connected to the ON/OFF power switch incorrectly.
Product
TAPSYSTEM Model 2A, REF 8002A
Manufacturer(s)
Cardiocommand Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →