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Late last month, Medtronic announced a voluntary recall of nearly 2,000 LIFEPAK 500 automated external defibrillators (AEDs), citing the possibility that these devices may continue to display a “connect electrodes” message and may not analyze the patient’s heart rhythm even when the electrodes are properly connected.
Complaints about an “increased level of indeterminate results from urine specimens stored with a urine processing pouch (UPP) at refrigerated temperatures” has led Becton Dickinson to voluntarily recall certain ProbeTec ET Urine Processing Kits from the global market.