Product Safety Recalls

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Philips Medical Systems DMC GmbH Recall 90490

Description: DigitalDiagnost C90 High Performance. radiography and fluoroscopy system

Philips Medical Systems DMC GmbH Recall 90490 Information

StatusOngoing
Mandated?FDA Mandated
Recall NumberZ-1328-2022
Event ID90490
Event DescriptionDigitalDiagnost C90 High Performance. radiography and fluoroscopy system
Product TypeDevices
DistributionUS Nationwide Distribution
Quantity120 systems in total
Recall ReasonFollowing 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.
Device Classification20220720
Device Code InfoModel 712034 Serial Numbers 10001073 10001104 10001108 10001109 10001119 10001126 10001135 10001140 10001144 10001145 10001153 10001156 10001157 10001163 10001170 10001173 10001178 10001179 10001183 10001191 10001192 10001199 10001200 10001201 10001203 10001208 10001210 10001216 10001220 10001231 10001232 10001234 10001235 10001236 10001240 10001241 10001248 10001251 10001261 10001262 10001264 10001270 10001271 10001273 10001275 10001280 21861349 21861369 21861402 21861418 21861456 21861460 21861471 21861475 21861490 21861496 21861497 21861498 21861501 21861502 21861525 21861531 21861542 22860038 22860118
Center Classification Date20220712
Recall Initiation Date20210519
Recalling FirmPhilips Medical Systems DMC GmbH
Initial Notification Letter
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