Product Recalls in Massachusetts

Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,530 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,530 in last 12 months

Showing 2838128400 of 52,647 recalls

Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT(R) ClearVUE(R) isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 6 Slice (Air) - Model no. 728256 Recalled by Philips Medical...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore (Radiology) - Model no. 728244 Recalled by Philips...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT - Model no. 728306 Computed Tomography X-Ray system Recalled...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core - Model no. 728321 Recalled by Philips Medical Systems...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT - Model no. 728332 Recalled by Philips Medical Systems...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 - Model no. 728231 Recalled by Philips Medical Systems...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT - Model no. 728326 Recalled by Philips Medical Systems...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Flex - Model no. 728317 Recalled by Philips Medical Systems...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Stanbio Laboratory, LP

Recalled Item: Stanbio AC power adapter for the HemoPoint H2 meter Recalled by Stanbio...

The Issue: The US prong (type A) adapter plate may crack, break, or detach and remain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing