Device recall
Z-1976-2019: TAPSYSTEM Model 2A, REF 8002A
FDA device recall · Class III · Cardiocommand Inc.
Key facts
| Recall number (Z-number) | Z-1976-2019 |
|---|---|
| Recall event | 83173 |
| Product | TAPSYSTEM Model 2A, REF 8002A |
| Product code | LPA |
| Recalling firm | Cardiocommand Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 1, 2021 |
| PMA numbers | P840002 |
| FEI number | 1927197 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database