Recall Z-2917-2011 ยท MKJ Automated External Defibrillators (Non-Wearable)
Cardiac Science Corporation
Automated External Defibrillator (non-wearable). Model number 9200, 9200N, 9200DN, 9200RD, 9210N, 9210RD, and CardioVive 92530. The battery component is warranted for 5 years, and electrodes have a shelf life of 2 years. The Powerheart AED G2 and CardioVive 92530 are intended to acquire the ECG rhythm for the detection of, and to provide treatment for, ventricular tachyarrhythmias of patients w
| Date | Aug 3, 2011 (initiated Jun 29, 2011) |
| Status | Terminated |
| Reason | Cardiac Science Corporation (CSC) intent to end service support and discontinue accessory sales of Powerheart G2 Automated External Defibrillators. Customers are recommended to choose a replacement AED prior to the current AED displaying any "Service Required" self test messages. |
| Root cause | Nonconforming Material/Component |
| Action | Cardiac Science Corporation (CSC) sent two "9200 SERIES CARDIAC SCIENCE AED NOTICE" letters dated August 2010 and March 2011 to all affected customers. The letters identifies the product, problem, and actions to be taken by the customers. Customers are encouraged to upgrade their devices through special offers by calling CSC at 800-426-0337, Option 2. For questions about the end of factory support for the affected devices, call the Technical Support team at 800-426-0337, Option 1. *****In August 2011, Cardiac Science sent out another updated recall notification letter to their consignees. |
| Quantity | 48,700 units (41396 units in US; 7304 units Internationally) |
| Distribution | Worldwide Distribution-USA (nationwide) and the countries of AE, AT, AU, AW, BE, BR, CA, CH, CL, CN, CO, CY, CZ, DE, OK, EG, ES, FI, FR, GB, HK, HR, HU, 10, IE, IL, IN, IR, IS, IT, JP, KR, KW, KY, LB, LT, LV, MT, MX, NG, NL, NO, NZ, PE, PF, PL, PR, PT, QA, RO, RU, SA, SG, SK, SY, TH, TR, TT, TW, VG |
| FDA record | Open on fda.gov |