LIFEPAK 20 defbrillator/monitor
This recall has been terminated (originally issued July 13, 2005).
- Recall Initiated
- June 17, 2005
- Posted
- July 13, 2005
- Terminated
- May 6, 2006
- Recall Number
- Z-0984-05
- Quantity
- 3924 units
- Firm Location
- Redmond, WA
- Official Source
- View on FDA website ↗
Reason for Recall
The defibrillator may not operate if the device is turned on during an AC Loss Alert.
Distribution
Devices were distributed to hospitals and medical centers worldwide.
Lot / Code Info
Various, noncontiguous serial numbers. Part numbers: 3202487-xxxd and 3202488-xxx.
Root Cause
Other
Action Taken
On 6/17/05 the firm issued a medical device correction letter to customers advising of the problem, explained what to do if the situation occurs, and that a service representative will visit and install new software.
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