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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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445 records meeting your search criteria returned- Product Code: MKJ Product Problem: Inappropriate/Inadequate Shock/Stimulation Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
PHILIPS NORTH AMERICA LLC FRX (W B) DEFIB, US ENGLISH, EXCHG 09/26/2021
PHILIPS NORTH AMERICA LLC HEARTSTART FRX DEFIB, US ENGLISH 09/24/2021
CARDIAC SCIENCE CORPORATION G3 PLUS, AED, AHA 2010, ENGLISH 09/20/2021
ZOLL MEDICAL CORPORATION ZOLL R-SERIES ALS DEFIBRILLATOR/MONITOR 09/07/2021
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 09/07/2021
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK(R) 20E DEFIBRILLATOR/MONITOR 08/30/2021
PHILIPS NORTH AMERICA LLC HEARTSTART FRX DEFIBRILLATOR 08/12/2021
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK 20 DEFIBRILLATOR/MONITOR 08/09/2021
PHILIPS NORTH AMERICA LLC HEARTSTART MRX MONITOR/DEFIB 08/05/2021
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK CR(R) PLUS DEFIBRILLATOR 08/04/2021
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