fda
2 records
FDA Recall: Physio Control, Inc. — Class II
20130731
The LIFEPAK 500 Automated External Defibrillator (AED) could be susceptible to malfunction due to an assembly error. If affected, the malfunction woul | Product: The LIFEPAK 500 Automated External Def...
View Source
FDA Device Recall: The LIFEPAK 500 Automated External Defibrillator is a semi-automatic defibrillat
2013-07-31
Class II — The LIFEPAK 500 Automated External Defibrillator (AED) could be susceptible to malfunction due to an assembly error. If affected, the malfunction would be the result of internal shorting on...
View Source
Be informed when major changes happen on C.F.A.I. — new data sources, platform updates, critical enforcement alerts
No spam. Only major updates. Unsubscribe anytime.