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Ultroid Technologies Recalls
4 recalls on record · December 28, 2016 to December 28, 2016 · Medical Devices
December 28, 2016Medical DevicesFDA
Ultroid Technologies, Inc. recalls Ultroid Sterile Disposable Probes sold individually
Hazard: Products are not designed, qualified, manufactured, and/or managed under a state of control per internal quality system procedures and external laws, regulations, directives, standards, and/or guidance (such as 21 CFR 820 Quality System Regulation)
December 28, 2016Medical DevicesFDA
Ultroid Technologies, Inc. recalls Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes.
Hazard: Products are not designed, qualified, manufactured, and/or managed under a state of control per internal quality system procedures and external laws, regulations, directives, standards, and/or guidance (such as 21 CFR 820 Quality System Regulation)
December 28, 2016Medical DevicesFDA
Ultroid Technologies, Inc. recalls Ultroid Mobile Generator/Battery operated unit including the Ultroid Sterile Disposable Probes
Hazard: Products are not designed, qualified, manufactured, and/or managed under a state of control per internal quality system procedures and external laws, regulations, directives, standards, and/or guidance (such as 21 CFR 820 Quality System Regulation)
December 28, 2016Medical DevicesFDA
Ultroid Technologies, Inc. recalls Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes
Hazard: Products are not designed, qualified, manufactured, and/or managed under a state of control per internal quality system procedures and external laws, regulations, directives, standards, and/or guidance (such as 21 CFR 820 Quality System Regulation)