Philips recalls HeartStart MRx defibrillators (models M3535A and M3536A) due to potential charging failure that could interrupt therapy. Affected units sold in the US from 2018-2020.
The MRx monitor/defibrillators could fail to charge because the therapy printed circuit board may have been loaded with an incorrect electronic component. Failure to charge could potentially cause therapy to be interrupted or delayed.
Philips is recalling two models of HeartStart MRx defibrillators because a faulty circuit board might cause the device to fail to charge. This could interrupt or delay life-saving therapy during cardiac emergencies.
The defibrillator's therapy printed circuit board may have an incorrect electronic component that prevents proper charging. If the device fails to charge, it could interrupt or delay critical life-saving therapy during cardiac emergencies.
Medical professionals who use these defibrillators for cardiac emergencies are most at risk. The recall affects specific models sold in the US between 2018 and 2020.
Check for model numbers M3535A (serial 861288) or M3536A (serial 861289) on the device. These models were sold in the US from 2018 to 2020.
Verify if your defibrillator has model numbers M3535A (serial 861288) or M3536A (serial 861289).
The defibrillator's therapy printed circuit board may have an incorrect electronic component that could cause it to fail to charge, potentially interrupting life-saving therapy.
No. The recall requires checking the model number and taking no action if the device is functioning properly.
Check the model number and serial number. If it matches the recalled models, contact Philips for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2035-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-2035-2018 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.
