Device evidence

device-recall:cfres:152589

The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR and the use of the LIFEPAK 1000 defibrillator.

Official recall number

Z-1257-2017

Evidence summary

Product code: MKJ
Recall status: Terminated
Event initiated: January 13, 2017
Root cause: Device Design
Source snapshot: d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product: Z-1257-2017