FDA Device recall Z-0792-2020
Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.)
- FDA Device
- Class II
- terminated
- Published 2020-01-15
On 2020-01-15 the FDA classified a Class II recall of Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.) by Cochlear Americas, citing product was packaged with the Incorrect tamper proof battery door.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0792-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-12-18 |
| Published | 2020-01-15 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Cochlear Americas |
| Distribution | CA, FL, IL, IN, MA, MO, NY, SD, TN, TX |
Product
Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.)
Reason
Product was packaged with the Incorrect tamper proof battery door.
Identifiers
| code_info | Part Number: P1129017 UDI Number: 09321502041096 Lot Number: COH1253733 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0792-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.