FDAMay 28, 2019device
ZOLL Pro-padz Liquid Gel Radiolucent, Part numbers: 8900-2105-01 (12/case) and 8900-2106-01 (single)
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Some of the electrodes may have been assembled incorrectly, preventing delivery of defibrillation or pacing therapy.
What to do
FDA enforcement status: Terminated
Brands named
bio detekbiobio detek
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- FDAMenopause Test Cassette (Urine)2025-11-22
- FDALH One Step Ovulation Test Device (Urine)2025-11-22
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