Day

April 24, 2002
Company: Zoll Medical CorpDate of Enforcement Report: 4/24/02 Class: I PRODUCT a) Zoll M Series Advisory Defibrillator. Recall # Z-0893-2; b) Zoll M Series AED Defibrillator (semi automatic defibrillator). Recall # Z-0894-2. REASON Defibrillator may fail to detect ventricular fibrillation and fail to deliver shock. CODE a) Serial Numbers: T98F00046-T01K27762 with System Software Version below...
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Company: Sunquest Information Systems, IncDate of Enforcement Report: 4/24/02 Class: II PRODUCT Misys Laboratory for Windows version 5.3. Recall # Z-0888-2. CODE REASON Software QA code of BOTH for patient sex can result in QA flags not being generated for abnormal results. Versions 5.3. RECALLING FIRM/MANUFACTURER Sunquest Information Systems, Inc., aka Misys Healthcare Systems Tucson,...
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