Class III — Cardiocommand Inc.
| Recalling firm | CARDIOCOMMAND, INC. |
|---|---|
| Registered facility | CARDIOCOMMAND, INC. (the firm's only registered facility) |
| Classification | Class III |
| Status | Terminated |
| Reason | 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 |
| Quantity | 6 units |
| Distribution | United States - AR, NM, PA, TX, and WA. |
| Initiated | 2019-06-24 |
| Classified | 2019-07-15 |
| Terminated | 2021-04-01 |
| Recall number | Z-1976-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class III recall — Cardiocommand Inc. (Z-1976-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83173/
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