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PTW NORTH AMERICA Recalls

1 recall on record · January 19, 2022 to January 19, 2022 · Medical Devices

January 19, 2022Medical DevicesFDA

PTW NORTH AMERICA CORPORATION recalls Software BeamAdjust version 2.2, Catalog No: S070009 Software VeriSoft version 8.0, Catalog No: S080032

Hazard: When a measurement with a PTW detector array is performed with the software BeamAdjust 2.2 or VeriSoft 8.0, a measurement error can occur under specific conditions. This error can lead to a too-low or too-high measured absolute dose which affects patient plan verification results

PTW NORTH AMERICA Recalls | RecallWatchUSA