Philips recalls QCPR meters used with HeartStart FR3 defibrillators due to risks of improper pad placement during CPR. Affected models include 861444, 861332, and others. Correct placement is critical for effective CPR.
Inform users of correct placement of the disposable adhesive pad on the QCPR meter and inform users of injuries associated with proper performance of CPR. As required by Consent Decree of Permanent Injunction No. 1:17-cv-11955-DJC, entered October 31, 2017 between United States of America and Philips North America
Philips is recalling QCPR meters that work with HeartStart FR3 defibrillators because improper pad placement during CPR could lead to ineffective resuscitation. This recall addresses a safety issue related to how the device is used to guide CPR techniques.
The QCPR meter provides feedback for CPR quality but requires correct placement of adhesive pads on the chest. If pads are placed incorrectly, the device may not guide rescuers effectively, potentially leading to ineffective CPR attempts during emergencies.
Rescuers using Philips QCPR meters with HeartStart FR3 defibrillators are most at risk if they don't follow proper pad placement instructions. The recall affects specific model numbers sold in the U.S. between 2017 and present.
Check for model numbers 861444, 861332, 989803139951, 989803162401, or 989803149941 on the QCPR meter. These meters are used with Philips HeartStart FR3 defibrillators or HeartStart MRx devices with specific software versions.
Review the device's instructions to ensure proper placement of adhesive pads on the chest for effective CPR.
Philips is recalling these meters to address risks of improper pad placement during CPR, which could lead to ineffective resuscitation attempts. This recall follows a court order from 2017.
Affected models include 861444, 861332, 989803139951, 989803162401, and 989803149941.
The recall does not require returning the device; users should follow proper pad placement instructions to ensure effective CPR.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0683-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-0683-2018 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.
