other medications. Recall Date: 02/03/2005 |
http://janrebel.eu/nextgen-image/116/91x68/crop/04a496fded6773155e72e470378d93ce Title: Certain Medtronic LIFEPAK 500 Automated External Defibrillators Class 1 Recall |
Units: LIFEPAK 500 automated external defibrillators (AEDs), part numbers 3005400-XXX, D3005400-XXX and U3005400-XXX. This action affects 1,924 devices. All were manufactured in 1997. |
Issue: The affected AEDs may display a “Connect Electrodes” message and then will not defibrillate the patient, even when the electrodes are properly connected. |