Device recall
Z-1315-2016: TeleSentry Battery, 3.7 Li-Ion Polymer Battery, CAUTION Do not expose to high…
FDA device recall · Class II · Scottcare Corporation
Key facts
| Recall number (Z-number) | Z-1315-2016 |
|---|---|
| Recall event | 73381 |
| Product | TeleSentry Battery, 3.7 Li-Ion Polymer Battery, CAUTION Do not expose to high temperature. Do not disassemble. Dispose of properly. Use specified charger only. 60pC/140pF The ScottCare Corporation. Intended for diagnostic evaluation of patients who experience transient symptoms or asymptomatic… |
| Product code | DSI |
| Recalling firm | Scottcare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 15, 2019 |
| 510(k) numbers | K092947 |
| FEI number | 1527715 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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