Devices

Device Recall MyLab Ultrasound System

Model / Serial
Software versions 4.0 - 13.60
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
US distribution in the states: AZ, FL, OK, PA, and TX.
Product Description
MyLab Ultrasound System; Models 6100, 6150, 6200, 6250; PA023E Probe 7.5/10
Manufacturer
ESAOTE S.P.A.
1 Event
- Recall of Device Recall MyLab Ultrasound System

Manufacturer

ESAOTE S.P.A.

Manufacturer Address
ESAOTE S.P.A., Sesto Fiorentino, Via Degli Olmi 11, Sesto Fiorentino Italy
Manufacturer Parent Company (2017)
Wansheng Medical Investments (Hong Kong) Limited
Source
USFDA

One device with a similar name

Learn more about the data here

Device Recall MyLab Ultrasound System

Model / Serial
Software versions 12.10 - 13.60
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
US distribution in the states: AZ, FL, OK, PA, and TX.
Product Description
MyLab Ultrasound System; Models 6100, 6150, 6200, 6250; Probes: BL433, C 18, CA541, EC1123, EC123, IH 618, IOT332, IOT342, L 415, LA332E, LA435, LA523, LA533, SI2C41, SL2325, TRT33
Manufacturer
ESAOTE S.P.A.

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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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