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. 2,710 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,710 in last 12 months

Showing 91619180 of 29,284 recalls

Medical DeviceSeptember 2, 2021· Abbott Molecular, Inc.

Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m Recalled by Abbott...

The Issue: There is a potential for false positive results.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 2, 2021· BioMerieux SA

Recalled Item: MYLA Versions: 4.7 Recalled by BioMerieux SA Due to Under certain...

The Issue: Under certain conditions, there is a risk for a false negative result.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2021· Abbott Molecular, Inc.

Recalled Item: Alinity m Resp-4-Plex AMP Kit (Non-US Assay) and Alinity m Recalled by...

The Issue: There is a potential for false positive results.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 2, 2021· Abbott Molecular, Inc.

Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Emergency Use Authorization Recalled by Abbott...

The Issue: There is a potential for false positive results.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 2, 2021· Abbott Molecular, Inc.

Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m Recalled by Abbott...

The Issue: There is a potential for false positive results.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 2, 2021· Abbott Molecular, Inc.

Recalled Item: Alinity m Resp-4-Plex AMP Kit (Emergency Use Authorization Recalled by...

The Issue: There is a potential for false positive results.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 31, 2021· Medtronic Xomed, Inc.

Recalled Item: Medtronic Sterile single-use blades that are components of the StraightShot...

The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2021· Medtronic Xomed, Inc.

Recalled Item: Medtronic sterile single-use blades that are components of the StraightShot...

The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2021· Medtronic Xomed, Inc.

Recalled Item: Medtronic sterile single-use blades that are components of the StraightShot...

The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force with software syngo.CT VB20 Model #10742326 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge with software syngo.CT VB20 Model #10590000 Recalled...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS with software syngo.CT VB20 Model #8098027 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash with software syngo.CT VB20 Model #10430603...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Confidence with software syngo.CT VB20 Model #10590100 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Drive with software syngo.CT VB20 Model #10431700 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK LOGIC Polyethylene Tibial Inserts Recalled by Exactech, Inc. Due to...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: ARTHROFOCUS Polyethylene Tibial Inserts (Product Line: 256-12-XX Recalled by...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: Vantage Total Ankle System including a. Vantage Fixed-Bearing Polyethylene...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing