Class II — Scottcare Corporation
| Recalling firm | ScottCare Corporation |
|---|---|
| Registered facility | SCOTTCARE CORPORATION (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The firm received a complaint of the battery exploding while recharging. |
| 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 events that may suggest cardiac arrhythmia. |
| Quantity | 9,067 batteries |
| Distribution | Worldwide Distribution -- USA, including the states of CA, CT, DE, FL, IL, KS, KY, MA, MD, MI, MN, MO, NC, NH, NJ, NM, NV, NY, OH, PA, SC, TN, TX, & WV; and, the country of Canada. |
| Initiated | 2016-02-25 |
| Classified | 2016-04-01 |
| Terminated | 2019-02-15 |
| Recall number | Z-1315-2016 |
| 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 II recall — Scottcare Corporation (Z-1315-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/73381/
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