Advanced Bionics Corporation Auria PowerPak, Model CI-7400-xxx where xxx denotes color/cable length options. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Auria PowerPak, Model CI-7400-xxx where xxx denotes color/cable length options.
Brand
Advanced Bionics Corporation
Lot Codes / Batch Numbers
All Codes.
Products Sold
All Codes.
Advanced Bionics Corporation is recalling Auria PowerPak, Model CI-7400-xxx where xxx denotes color/cable length options. due to Battery pack may overheat and cause patient burns.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Battery pack may overheat and cause patient burns.
Recommended Action
Per FDA guidance
Notification letters were sent to all users and affiliates on July 27, 2004. Initially customers were informed that they will receive a retrofit kit. Firm decided to actually recall the battery packs and sent recall letters on August 10, 2004. All Auria Battery Packs are to be returned per instructions in the recall letters. Firm rerecalled powerpaks that had been repaired since FDA review has found that repairs are not sufficent to address all potential adverse events concieveable. The latest recall letter was sent May 11-12, 2005
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026