Philips Medical Systems Philips HeartStart FRx Defibrillator, Automated External Defibrillator (AED), catalog number 861304. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Philips HeartStart FRx Defibrillator, Automated External Defibrillator (AED), catalog number 861304.
Brand
Philips Medical Systems
Lot Codes / Batch Numbers
Serial Number: B08G-01884
Products Sold
Serial Number: B08G-01884
Philips Medical Systems is recalling Philips HeartStart FRx Defibrillator, Automated External Defibrillator (AED), catalog number 861304. due to The affected device may not deliver appropriate defibrillation therapy.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The affected device may not deliver appropriate defibrillation therapy.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026