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. 2,520 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,520 in last 12 months

Showing 3486134880 of 52,647 recalls

Medical DeviceJuly 19, 2016· Philips Electronics North America Corporation

Recalled Item: MultiDiagnost Eleva with Flat Detector Recalled by Philips Electronics North...

The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2016· Philips Electronics North America Corporation

Recalled Item: UroDiagnost Recalled by Philips Electronics North America Corporation Due to...

The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2016· Philips Electronics North America Corporation

Recalled Item: MultiDiagnost Eleva Recalled by Philips Electronics North America...

The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Whipknot Soft Tissue Cinch (USP#5) suture. PN: Recalled by...

The Issue: Sterility compromised due to breach in sterile packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Aribex Inc

Recalled Item: NOMAD Pro Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...

The Issue: Firm received customer complaints where end users reported that Nomad Pro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Sofamor Danek USA Inc

Recalled Item: TIBIAL TRAY Recalled by Medtronic Sofamor Danek USA Inc Due to The alpha...

The Issue: The alpha total knee replacement components that may have not been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-330NR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: MACH Cranial Treon. The software application is sent in CD format with an...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Sofamor Danek USA Inc

Recalled Item: RESPONSIVE Recalled by Medtronic Sofamor Danek USA Inc Due to The alpha...

The Issue: The alpha total knee replacement components that may have not been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Sofamor Danek USA Inc

Recalled Item: TIBIAL TRAY Recalled by Medtronic Sofamor Danek USA Inc Due to The alpha...

The Issue: The alpha total knee replacement components that may have not been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Sofamor Danek USA Inc

Recalled Item: RESPONSIVE Recalled by Medtronic Sofamor Danek USA Inc Due to The alpha...

The Issue: The alpha total knee replacement components that may have not been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: MACH AxiEM Cranial Treon. The software application is sent in Recalled by...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Sofamor Danek USA Inc

Recalled Item: TIBIAL TRAY Recalled by Medtronic Sofamor Danek USA Inc Due to The alpha...

The Issue: The alpha total knee replacement components that may have not been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-450NR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Sofamor Danek USA Inc

Recalled Item: RESPONSIVE Recalled by Medtronic Sofamor Danek USA Inc Due to The alpha...

The Issue: The alpha total knee replacement components that may have not been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Sofamor Danek USA Inc

Recalled Item: RESPONSIVE Recalled by Medtronic Sofamor Danek USA Inc Due to The alpha...

The Issue: The alpha total knee replacement components that may have not been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-330BR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Aribex Inc

Recalled Item: NOMAD Pro2 Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...

The Issue: Firm received customer complaints where end users reported that Nomad Pro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-450BR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Sofamor Danek USA Inc

Recalled Item: TIBIAL TRAY Recalled by Medtronic Sofamor Danek USA Inc Due to The alpha...

The Issue: The alpha total knee replacement components that may have not been...

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

Class II — Potential Health HazardOngoing