medical Class II Updated 2022-07-20

Philips Medical Systems DMC GmbH recalls DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fl

Recalled Product

DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fluoroscopy system


Hazard / Issue

Following a system restart where the Table Height 2 (TH2) is the default setting and then switched to Wallstand VS2, operators will see an incorrect orientation of image on the first examination due to an issue in the firmware of the Wallstand VS2 board. The system will rotate the amplimat field selection by 90 degrees. The wrong amplimat field selection may cause an incorrect dose of radiation to occur. Additionally, the anatomic position markers may become mispositioned and could potentially be associated with the opposite side of the anatomy. (Updated 1/30/23) Expansion of the root cause to include incorrect amplimat field selection by 90 degrees following the first exposure using Wallstand VS2 and a subsequent system restart. Previously, this issue only occurred following a system restart where the Table Height 2 (TH2) is the default setting.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Model 712035 Serial Numbers 21862105 21862107 21862123 21862126 22860027
View official government recall

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