Cochlear Baha 5 Sound Processor Tamper Proof Battery Door — Class II medical device recall Z-0792-2020
Terminated recall by Cochlear Americas Inc., reported 2020-01-15, distributed in CA, FL, IL, IN, MA, MO, NY, SD…. Product was packaged with the Incorrect tamper proof battery door.
| Recall number | Z-0792-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cochlear Americas Inc., Centennial, CO, United States |
| Recall initiated | 2018-12-18 |
| Classified | 2020-01-09 |
| Reported by FDA | 2020-01-15 |
| Terminated | 2021-01-28 |
| Distributed | CA, FL, IL, IN, MA, MO, NY, SD, TN, TX |
| Quantity | 50 units |
| UPC / GTIN / UDI-DI | 09321502041096 |
| Lot numbers | COH1253733 |
| Model numbers | P1129017 |
Product
Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.)
Reason for recall
Product was packaged with the Incorrect tamper proof battery door.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0792-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.