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Combolab altix
Official notice
21 Aug 2023
Last checked
21 Aug 2023
An official Health Canada notice concerns Combolab altix. GE Healthcare has become aware that a diode on the power supply of the Prucka 3 Amplifier used with cardiolab/combolab systems could reach elevated temperatures. This could cause the amplifier to fail and consequently power off and become inoperable. Recall Start Date: August 8, 2023 Published 2023-08-21.
What to do now
Contact the manufacturer if you require additional information.
Recall number
74139
Official notice
2023-08-21
The hazard
The hazard
GE Healthcare has become aware that a diode on the power supply of the Prucka 3 Amplifier used with cardiolab/combolab systems could reach elevated temperatures. This could cause the amplifier to fail and consequently power off and become inoperable. Recall Start Date: August 8, 2023
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
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Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: GE Medical Information, Combolab Altix.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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