FDA Device recall Z-1083-2019
Na¿da CL Q30 Sound Processor, Sand Beige, Model Cl-5260-120
- FDA Device
- Class II
- terminated
- Published 2019-04-10
On 2019-04-10 the FDA classified a Class II recall of Na¿da CL Q30 Sound Processor, Sand Beige, Model Cl-5260-120 by Advanced Bionics, citing the sound processors were loaded with the incorrect firmware.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1083-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-02-06 |
| Published | 2019-04-10 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Advanced Bionics |
| Distribution | NC |
Product
Na¿da CL Q30 Sound Processor, Sand Beige, Model Cl-5260-120; Silver Gray, Model Cl-5260-140; and Velvet Black, Model Cl-5260-150.
Reason
The sound processors were loaded with the incorrect firmware.
Identifiers
| code_info | Model Cl-5260-120 - Serial number 1047584, UDI (01)07630016838057(11)180309(21)1045784; Model Cl-5260-140 - Serial…Model Cl-5260-120 - Serial number 1047584, UDI (01)07630016838057(11)180309(21)1045784; Model Cl-5260-140 - Serial number 1047481, UDI (01)07630016829710(11)151208(21)1047481; and Serial number 1047482, UDI (01)07630016829710(11)151208(21)1047482; and Model Cl-5260-150 - Serial number 1082276, UDI (01)07630016838071(11)180925(21)1082276. |
|---|
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-1083-2019%22
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