Philips recalls HeartStart XL+ Defibrillator Model 861290 that may fail to turn on or restart unexpectedly, rendering it unable to return to ready state. Affected units may not function properly during self-tests.
Device may fail to turn on or unexpectedly attempt to restart, rendering it unable to return to a ready for use state. Additionally, this issue may occur when the device is in standby mode, when attempting to power on to run a self-test. If this occurs, the device will indicate that it is not ready for use.
Philips is recalling HeartStart XL+ Defibrillator monitors with model number 861290 because they may fail to turn on or restart unexpectedly, making them unable to return to a ready state for use. This could prevent the device from functioning properly during critical medical situations.
The device may fail to turn on or unexpectedly restart when in standby mode, preventing it from returning to a ready state. This issue can occur during self-tests or when attempting to power on the device. If this happens, the device will show it is not ready for use.
Healthcare professionals who use the HeartStart XL+ Defibrillator monitors with model number 861290 are most at risk. The recall affects all units sold with this specific model number.
Check for the model number 861290 on the device. All units with this model number are affected by the recall.
Ensure the device shows it is ready for use by attempting to power on and running a self-test.
No, this recall specifically affects model number 861290. Other models are not included.
If the device fails to turn on or shows it is not ready for use, stop using it and contact Philips for further instructions.
Check the model number on the device; if it is 861290, it is affected by this recall.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0608-2020 — Philips Philips Hello, I own a Philips that is covered by recall Z-0608-2020 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.
