Philips recalls HeartStart XL+ Defibrillator Model 861290 made before May 2017 due to potential failure of the therapy selector switch causing unexpected device behavior.
The rotary therapy selector switch may fail, resulting in unexpected device behavior. These behaviors include: The device may not turn on; The device may not perform the selected function; The device may deliver a shock with an energy level different from the setting selected by the user.
Philips is recalling HeartStart XL+ Defibrillator monitors made before May 2017 because the therapy selector switch might fail, leading to the device not turning on, not performing selected functions, or delivering shocks at incorrect energy levels. This could affect medical use safety.
The therapy selector switch may fail, causing the device to not turn on, not perform the selected function, or deliver shocks with incorrect energy levels. This could lead to improper medical treatment during emergencies.
Medical professionals using the HeartStart XL+ Defibrillator monitors are most at risk. Patients receiving care with these devices could be affected if the device malfunctions.
Check for the model number 861290 on the device. Units were manufactured before May 2017 and sold in the United States.
Look for the model number 861290 on the device to confirm if it is recalled.
Reach out to Philips customer support for guidance on next steps if the device is recalled.
The therapy selector switch may fail, causing the device to not turn on, not perform the selected function, or deliver shocks with incorrect energy levels.
Model 861290, manufactured before May 2017.
Check for the model number 861290 on the device and verify it was manufactured before May 2017.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0498-2020 — Philips Philips Hello, I own a Philips that is covered by recall Z-0498-2020 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.
