Philips recalls HeartStart FRx defibrillators with model 861304 due to unreported prior recalls. Affected units may have missed previous safety notices.
Customers were not notified of previous recalls associated with various defibrillator models.
Philips is recalling HeartStart FRx defibrillators with model number 861304 because previous recalls for these devices were not properly notified to customers. This means some users might not have been aware of earlier safety issues.
The hazard comes from the fact that customers were not informed about earlier recalls for these defibrillator models. This could mean that some users might have been using devices that had already been recalled but were unaware of the need to stop using them.
Healthcare professionals and emergency responders who use Philips HeartStart FRx defibrillators with model 861304 are most at risk. This recall affects devices that were previously part of other recalls but were not properly notified.
Check for model number 861304 on the defibrillator. Serial numbers include 0805164058, B12C-03067, B07I-01107, B09D-01464, B08L-00595, or B10I-03918.
Look for model number 861304 on the defibrillator to confirm if it is affected.
This recall is because previous recalls for these defibrillator models were not properly notified to customers.
The recall does not require immediate action, but you should check if your device has model number 861304 and serial numbers listed above.
The hazard is that customers were not informed about earlier recalls, which could mean some users might have been using devices that had already been recalled.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0079-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-0079-2022 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
