Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ZOLL Pro-padz Liquid Gel Radiolucent Recalled by Bio-Detek, Inc. Due to Some of the electrodes may have been assembled...
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 Bio-Detek, Inc. directly.
Affected Products
ZOLL Pro-padz Liquid Gel Radiolucent, Part numbers: 8900-2105-01 (12/case) and 8900-2106-01 (single)
Quantity: 1789
Why Was This Recalled?
Some of the electrodes may have been assembled incorrectly, preventing delivery of defibrillation or pacing therapy.
Where Was This Sold?
This product was distributed to 13 states: AZ, CA, CO, CT, FL, LA, MN, NV, OH, PA, TN, UT, WY
About Bio-Detek, Inc.
Bio-Detek, Inc. has 9 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