Philips HeartStart FRx Defibrillator, Automated External Defibrillator (AED), catalog number 861304.
This recall has been terminated (originally issued November 22, 2010).
- Company
- Philips Medical Systems
- Recall Initiated
- August 7, 2008
- Posted
- November 22, 2010
- Terminated
- December 1, 2010
- Recall Number
- Z-0432-2011
- Quantity
- 1 unit
- Firm Location
- Seattle, WA
- Official Source
- View on FDA website ↗
Reason for Recall
The affected device may not deliver appropriate defibrillation therapy.
Distribution
Nationwide Distribution: to one account in Arkansas.
Lot / Code Info
Serial Number: B08G-01884
Root Cause
Employee error
Action Taken
Philips notified the customer with the affected device by phone on August 8, 2008 . A replacement device was shipped to the customer on August 11, 2008.
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