Class II — Cochlear Americas Inc.
| Recalling firm | COCHLEAR AMERICAS |
|---|---|
| Registered facility | View this company's 7 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Product was packaged with the Incorrect tamper proof battery door. |
| Product | Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.) |
| Quantity | 50 units |
| Distribution | Domestic: CA, FL, IL, IN, MA, MO, NY, SD, TN, and TX OUS Regions; Asia Pacific (APAC), and Europe, The Middle East and Africa (EMEA) |
| Initiated | 2018-12-18 |
| Classified | 2020-01-09 |
| Terminated | 2021-01-28 |
| Recall number | Z-0792-2020 |
| 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 — Cochlear Americas Inc. (Z-0792-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83970/
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