# FDA recall Z-1083-2019

> **Advanced Bionics, LLC** · Class II · device recall initiated 2019-02-06.

## 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 for recall

The sound processors were loaded with the incorrect firmware.

## Distribution

Distribution was made to NC.  Foreign distribution was made to Canada, Argentina, Germany, South Africa, Egypt, Kuwait, and Iran.  There was no government/military distribution.

## Key facts

- **Recall number:** Z-1083-2019
- **Recalling firm:** Advanced Bionics, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-02-06
- **Report date:** 2019-04-10
- **Termination date:** 2024-02-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Valencia, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1083-2019

## Citation

> AI Analytics. FDA recall Z-1083-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1083-2019. Source: US FDA. Licensed CC0.

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