Devices

Philips HeartStart XL+ Defibrillator/Monitor

Model / Serial
Model: HeartStart XL+, Affected: Manufactured between Oct-2011 and Jan-2013
Manufacturer
Philips Medical Systems (USA)
1 Event
- Recall of Philips HeartStart XL+ Defibrillator/Monitor

Manufacturer

Philips Medical Systems (USA)

Manufacturer Parent Company (2017)
Philips
Source
NZMMDSA

9 devices with a similar name

Learn more about the data here

Philips HeartStart XL+ Defibrillator/Monitor

Model / Serial
Model: Model number: 861290, Affected: , Software version: Units upgraded to B.00.01 software, or manufactured by Philips between December, 2013 and February, 2014
Manufacturer
Philips Medical Systems (USA)

Philips HeartStart XL+ Defibrillator/Monitor

Model / Serial
model number 861290 Units Affected: Units manufactured by Philips from October, 2011 to January 2013, and shipped worldwide with serial numbers within the ranges: USO1100100 – USO1100372 USN1100376 – USN1100960 USD1100961 – USD1101095 US11201096 – US11201186 US21201187 – US21201239 US31201240 – US31201537 US41201538 – US41201585 US51201586 – US51201721 US61201722 – US61201924 US71201925 – US71202048 US81202049 – US81202168 US91202169 – US91202514 USO1202515 – USO1202990 USN1202991 – USN1203537 USD1203538 – USD1203968 US11303969 – US11303972
Product Description
Defibrillator/Monitor
Manufacturer
Philips Healthcare

the Philips HeartStart XL+ Defibrillator/Monitor

Model / Serial
Product Description
Medical electronics / Electromedical devices - electrotherapy
Manufacturer
Philips Healthcare

Philips HeartStart XL+ Defibrillator/Monitor

Model / Serial
Product Description
Medical electronics / Electromedical devices - electrotherapy
Manufacturer
Philips Healthcare

Philips HeartStart XL+ Defibrillator/Monitor

Model / Serial
Product Description
Philips HeartStart XL+ Defibrillator/Monitor
Manufacturer
Philips Electronics (S) Pte Ltd

4 more

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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