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. 2,706 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,706 in last 12 months

Showing 1012110140 of 52,647 recalls

Medical DeviceMarch 1, 2023· Stryker Corporation

Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 34X4...

The Issue: Not able to achieve desired pressure and not holding pressure result from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2 and LifeVentEVO2 Portable Electric Ventilator Recalled by...

The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2023· Stryker Corporation

Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 18X4...

The Issue: Not able to achieve desired pressure and not holding pressure result from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Elekta Instrument AB

Recalled Item: Instructions for Use for the following Leksell Stereotactic System and...

The Issue: The incorrect IFU was distributed with the devices.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Atrium Medical Corporation

Recalled Item: Express Mini 500 Dry Seal Chest Drain Recalled by Atrium Medical Corporation...

The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Stryker Sustainability Solutions

Recalled Item: Color Cuff Single Port Recalled by Stryker Sustainability Solutions Due to...

The Issue: Increased incidence of disposable tourniquet cuffs "not able to achieve...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Atrium Medical Corporation

Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...

The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 28, 2023· Sagent Pharmaceuticals Inc

Recalled Item: Heparin Sodium Injection Recalled by Sagent Pharmaceuticals Inc Due to...

The Issue: Labeling: Not elsewhere classified

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 28, 2023· Omega Medical Imaging, Inc.

Recalled Item: Omega Medical Imaging Elevating Monitor Suspension Recalled by Omega Medical...

The Issue: An actuator separated from the pivot mechanism on a lower monitor boom...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to APLS IgM reagent...

The Issue: APLS IgM reagent kits were packaged with the incorrect conjugate, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Bard Peripheral Vascular Inc

Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM Recalled by...

The Issue: The external diameter of the biopsy instrument is larger than the internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Elekta Inc

Recalled Item: Monaco RTP System. Used to make treatment plans for patients Recalled by...

The Issue: Re-optimization, after adding contours without forced density outside the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2023· FUJIFILM Healthcare Americas Corporation

Recalled Item: FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system Recalled...

The Issue: Arm which holds the tube head in place is susceptible to breaking, if the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 24, 2023· Global Pharma Healthcare Private Limited

Recalled Item: Delsam Pharma's Artificial Eye Ointment (Mineral Oil 15% Recalled by Global...

The Issue: Non-Sterility: FDA analysis found unopened tubes to be contaminated with...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment...

The Issue: CGMP DEVIATIONS

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Alcolado Relampago (menthol 1% Recalled by Ecometics, Inc. Due to CGMP...

The Issue: CGMP DEVIATIONS

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Activator Concentrate (sodium fluoride 0.96% in Activator) 1 fl. Oz Recalled...

The Issue: CGMP DEVIATIONS

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Vencedor medicated balm (capsaicin 0.028%) 1.5 oz. (43g) tubes Recalled by...

The Issue: CGMP DEVIATIONS

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Unguentine Original Ointment for Burns (Camphor 3.0% Recalled by Ecometics,...

The Issue: CGMP DEVIATIONS

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Soltice Quick-RUB (Menthol 5.1% Recalled by Ecometics, Inc. Due to CGMP...

The Issue: CGMP DEVIATIONS

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund