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. 2,765 recalls have been distributed to Massachusetts in the last 12 months.
Showing 621–640 of 52,647 recalls
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter UniCel Dxl 600 Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter has determined that, due to a potential communication issue,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter UniCel Dxl 800 Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter has determined that, due to a potential communication issue,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...
The Issue: Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Dietary Supplement...
The Issue: Undeclared milk allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Celebration Herbals Senna Leaf Herbal Tea 24 Teabags Recalled by CELEBRATION...
The Issue: possible salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive...
The Issue: Butyrate tube cracks during actuation, rendering product unusable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zen Cleanse Blend herbal tea Recalled by Bell Industries LLC Due to...
The Issue: Potential Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FreeStyle Libre 3 Sensor UDI-DI code: 00357599818005 The Recalled by Abbott...
The Issue: Due to a manufacturing process issue that may cause carbon build up in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outer-packaging: gimme! brand Decaf de Agua coffee pods Recalled by Gimme...
The Issue: Undeclared caffeine
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FreeStyle Libre 3 Plus Sensor UDI-DI code: 00357599844011 Recalled by Abbott...
The Issue: Due to a manufacturing process issue that may cause carbon build up in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 3 Plus Sensor UDI-DI code: 00357599843014 Recalled by Abbott...
The Issue: Due to a manufacturing process issue that may cause carbon build up in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 3 Plus Sensor UDI-DI code: 00357599819002 Recalled by Abbott...
The Issue: Due to a manufacturing process issue that may cause carbon build up in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeShield Drug Library Management (DLM) Recalled by ICU Medical, Inc. Due...
The Issue: For certain customers, the Change Summary review option ceases to operate as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Vapor 2000. Unheated Recalled by Draeger, Inc. Due to A certain...
The Issue: A certain component of affected devices was not delivered within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.