Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Na¿da CI Q90 Sound Processor Recalled by Advanced Bionics, LLC Due to The sound processors were loaded with the incorrect...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Advanced Bionics, LLC directly.
Affected Products
Na¿da CI Q90 Sound Processor, Silver Gray, Model Cl-5280-140.
Quantity: 1 sound processor
Why Was This Recalled?
The sound processors were loaded with the incorrect firmware.
Where Was This Sold?
This product was distributed to 1 state: NC
About Advanced Bionics, LLC
Advanced Bionics, LLC has 11 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report