Philips recalls QCPR meters used with HeartStart devices due to risks of improper pad placement during CPR. Affected units include specific model numbers sold with HeartStart FR3 or MRx devices.
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 defibrillators because incorrect pad placement during CPR could lead to injuries. This recall is part of a legal requirement to ensure proper CPR technique.
The QCPR meter requires correct placement of adhesive pads on the chest to provide accurate CPR feedback. Improper placement could cause injuries during CPR attempts, especially if the device is used incorrectly.
People using Philips QCPR meters with HeartStart FR3 or MRx defibrillators are affected. Rescuers performing CPR with these devices are most at risk if they place the pads incorrectly.
Check for model numbers 861444, 861332, 989803139951, 989803162401, or 989803149941 on the QCPR meter. These units were sold with HeartStart FR3 defibrillators (software version PR2.0 or higher) or HeartStart MRx devices (software version F.01/R.01 or F.02/R.02).
Ensure the adhesive pads are correctly placed on the chest as per the device instructions to avoid injury during CPR.
This recall is required by a court order to ensure proper CPR technique and prevent injuries from incorrect pad placement.
The affected models are 861444, 861332, 989803139951, 989803162401, and 989803149941.
No return is required; users should check pad placement to ensure safe CPR use.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0684-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-0684-2018 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.
