Manufacturer
2 recalls in our database name Cardiac Science Corporation as the manufacturing or recalling firm.
Of the 2 recalls from Cardiac Science Corporation we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Cardiac Science is recalling five Powerheart G5 AEDs because sub-supplier documentation is insufficient to verify that the printed circuit boards conform to specifications.
Cardiac Science is recalling specific defibrillation electrodes that may develop high electrical impedance, causing AED self-test failures.