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Regulatory Insight Recalls

1 recall on record · March 2, 2016 to March 2, 2016 · Medical Devices

March 2, 2016Medical DevicesFDA

Regulatory Insight, Inc recalls GE Precision MPi is an all-digital multipurpose tilt-C x-ray system, intended for a multitude of diagnostic procedures,

Hazard: It was discovered that the Remote Touch Panel (RTP) of the GE Precision MPi X-ray system may not always boot up as intended and needs to be updated to properly accomplish its intended purpose.

Regulatory Insight Recalls | RecallWatchUSA