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 85818600 of 29,284 recalls

Medical DeviceFebruary 11, 2022· Huntleigh Healthcare Ltd.

Recalled Item: HUNTLEIGH Disposable intraoperative Probe Recalled by Huntleigh Healthcare...

The Issue: Faceplate may become detached from the probe body.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2022· RaySearch America Inc

Recalled Item: RayStation 4-11B Recalled by RaySearch America Inc Due to Incorrect source...

The Issue: Incorrect source to skin or surface distance (SSD) calculation may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2022· Abbott Molecular, Inc.

Recalled Item: Alinity m Integrated Reaction Units (IRU) Recalled by Abbott Molecular, Inc....

The Issue: There is potential for the Reaction Vessels (RVs) detaching from the RV cap...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· bioMerieux, Inc.

Recalled Item: VIDAS CMV IgM Recalled by bioMerieux, Inc. Due to Invalid calibrations (out...

The Issue: Invalid calibrations (out of range high) while using the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Fructosamine (Fruc) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Enzymatic Hemoglobin A1c (A1c_E/A1c_H) Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Calcium_2 (CA_2) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2022· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 SYPH T PACK Syphilis Total & RPR Reagent Pack Recalled by...

The Issue: Due to current concerns related to COVID-19 vaccine interference with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2022· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Syphilis Total & RPR Calibrator Set CAL Recalled by Bio-Rad...

The Issue: Due to current concerns related to COVID-19 vaccine interference with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2022· Philips North America, LLC

Recalled Item: The IFU for the Autoclavable Temperature Probes: Part # 453564635891...

The Issue: Update to instructions for use regarding the cleaning and disinfection...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2022· Brius Technologies Inc.

Recalled Item: Brius Patient Specific Brackets (components in a set of custom Recalled by...

The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2022· Brius Technologies Inc.

Recalled Item: Customized Brius Appliances (custom metal orthodontic devices) Recalled by...

The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2022· Brius Technologies Inc.

Recalled Item: Brius Pontics (components in a set of custom metal orthodontic devices)...

The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2022· B Braun Medical Inc

Recalled Item: PERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump Recalled by...

The Issue: Units not properly inspected prior to release to the market, may not...

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

Class II — Potential Health HazardOngoing