Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
TAPSYSTEM Model 2A Recalled by Cardiocommand Inc. Due to There is a potential for an assembly error...
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 Cardiocommand Inc. directly.
Affected Products
TAPSYSTEM Model 2A, REF 8002A
Quantity: 6 units
Why Was This Recalled?
There is a potential for an assembly error resulting in the battery wire being connected to the ON/OFF power switch incorrectly.
Where Was This Sold?
This product was distributed to 5 states: AR, NM, PA, TX, WA
About Cardiocommand Inc.
Cardiocommand Inc. has 2 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