Reported Feb 27, 2013 · Terminated
Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The HeartStart XL+ is intended for use in a hospital…
Philips Healthcare Inc.
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: Philips Healthcare Inc. · 3000 Minuteman Road · Andover, MA · 01810
Is this the product you have?
- Philips HeartStart XL+
- Defibrillator/Monitor Model number861290 The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or defibrillation
- Lot codes and dates
- Serial number range
USO1100100 - USO1100372USN1100376 - USN1100960USD1100961 - USD1101095US11201096 - US11201186US21201187 - US21201239US31201240 - US31201537US41201538 - US41201585US51201586 - US51201721US61201722 -US61201924US71201925 - US71202048US81202049 - US81202168US91202169- US91202514USO1202515 - USO1202990USN1202991 - USN1203537USD1203538- USD1203968US11303969 - US11303972
- Serial number range
- Amount recalled
- 3785 units
Where it was sold
- Nationwide
Why it was recalled
Philips HeartStart XL+ Defibrillator/Monitor may become locked out of clinical use
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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