Devices

Device Recall Cardiovive 92531 automated external defibrillator

Model / Serial
SERIAL NUMBERS: 331327, 331014, 331000, 331317, 330984, 341805, 341827, 341306, 341912, 338527, 341683, 335085, 338117, 341312, 340263, 341818, 341820, 341821, 341791, 341890, 338113, 338059, 341944, 338039, 338041, 335057, 341348, 338084, 338053, 341782, 338060, 341923, 338073, 338075, 341316, 340255, 338050, 340365, 341787, 341732, 341729, 341726, 340354, 338078, 341717, 338916, 341882, 341703, 341263, 341706, 335258, 338142, 341877, 340312, 341780, 341778, 338217, 341836, 338940, 340338, 335140, 341884, 341755, 334495, 341750, 341749, 341891, 338035, 334402, 335413, 341497, 338024, 335457, 341966, 341534, 338002, 341518, 341430, 338017, 341511, 338027, 341548, 341566, 341567, 341542, 341434, 335449, 341549, 381727, 381729, 381724, 341888, 341806, 341901, 338079 and 341790.
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
No
Distribution
Worldwide Distribution -- UNITED STATES, ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, BAHAMAS, BAHRAIN, BELARUS, BELGIUM, BERMUDA, BOLIVIA, BRAZIL, BULGARIA, CANADA, CAYMAN ISLANDS, CHILE, CHINA, COLOMBIA, COSTA RICA, CROATIA, CYPRUS, CZECH REPUBLIC, CZECHOSLOVAKIA, DENMARK, DOMINICAN REPUBLIC, ECUADOR, EGYPT, EL SALVADOR, FINLAND, FRANCE, GERMANY, GRECE, GUAM, GUATEMALA, HOLLAND, HONDURAS, HONG KONG, HUNGARY, ICELAND, INDIA, INDONESIA, IRAQ, IRELAND, ISRAEL, ITALY, JAMAICA, JAPAN, JORDAN, KENYA, KOREA, KUWAIT, LEBANON, LIBYA, LITHUANIA, MALAYSIA, MALTA, MEXICO, MONACO, MORROCCO, NAMIBIA, NETHERLANDS, NEW CALEDONIA, NEW ZEALAND, NIGERIA, NORWAY, OMAN, PAKISTAN, PANAMA, PARAGUAY, PERU, PHILIPPINES, POLAND, PORTUGAL, PUERTO RICO, QATAR, ROMANIA, RUSSIA, SAUDI ARABIA, SCOTLAND, SERBIA, SINGAPORE, SLOVAKIA, SLOVENIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, THAILAND, TRINIDAD & TOBAGO, TURKEY, UAE, UKRAINE, UNITED KINGDOM, URUGUAY, VENEZUELA, VIETNAM, VIRGIN ISLANDS AND YEMEN.
Product Description
Burdick Cardiovive 92531 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). || Intended for use in either in-hospital or out-of-hospital settings for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing.
Manufacturer
Cardiac Science Corporation
1 Event
- Recall of Device Recall Cardiovive 92531 automated external defibrillator

Manufacturer

Cardiac Science Corporation

Manufacturer Address
Cardiac Science Corporation, 3303 Monte Villa Pkwy, Bothell WA 98021-8969
Manufacturer Parent Company (2017)
Cardiac Science Corporation
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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