Reported Apr 9, 2014 · Terminated
Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Version 02.10.02.00 or…
ZOLL Medical Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: ZOLL Medical Corporation · 269 Mill Road · Chelmsford, MA · 01824
Is this the product you have?
- Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Version 02.10.02.00 or Higher, automated external defibrillator.
- Lot codes and dates
- System Software Version 02.10.02.00 or Higher
- Amount recalled
- 3,169 units
Where it was sold
- Nationwide
Why it was recalled
Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop and cannot be used
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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