FDAClass IIIDecember 2, 2020

AB PowerCel 230 recall: Labeling Error

AB PowerCel 230 (velvet black), REF: CI-5523-150, UDI: (01) 07630016832956 used to power the following devices: Na¿da CI Q90 Sound Processor…

Why was AB PowerCel 230 recalled?

Mislabeling; It has been determined that some batteries were improperly labeled and may contain a different battery life than indicated.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

410079020

Product
AB PowerCel 230 (velvet black), REF: CI-5523-150, UDI: (01) 07630016832956 used to power the following devices: Na¿da CI Q90 Sound Processor…
Recalling firm
Advanced Bionics, LLC
Quantity
53 units
Distribution
Worldwide distribution - US Nationwide distribution including in the states of NY, IL, MA, NE, CA, HI, LA, MS, AL, FL, SC, OH and the countries of Belgium, Germany, Italy Netherlands, Spain, Colombia, Czech Republic, Iran, Kuwait, Panama, Peru, Taiwan, Italy.
Recall date
December 2, 2020
Classification
Class III
Status
Terminated
Agency
FDA (device)
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