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. 2,730 recalls have been distributed to Massachusetts in the last 12 months.
Showing 4941–4960 of 29,284 recalls
Recalled Item: BD BBL Sensi Disc Minocycline - 30 ug Recalled by Becton Dickinson & Co. Due...
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-RF-32-USA RotaFlow Centrifugal Pump with BIOLINE Coating Recalled by...
The Issue: Nonconformities at their seal could potentially compromise the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Sensi Disc Tetracycline 30 ug Recalled by Becton Dickinson & Co. Due...
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensi Disc Amoxicillin with Clavulanic Acid 20/10 ¿g Recalled by Becton...
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Sensi Disc Ampicillin with Sulbactam 10/10 ¿g Recalled by Becton...
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet) Recalled...
The Issue: The negative control was contaminated with one of the positive control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Sensi Disc Ciprofloxacin- 5 ug Recalled by Becton Dickinson & Co. Due...
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTIMIZER model CCM X11 implantable pulse generator (IPG) devices - Recalled...
The Issue: OPTIMIZER devices may cease to deliver CCM therapy if the device incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Contro-Bulb Syringe Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Packaging material was updated for the Bulb Irrigation Syringe (DYND20125),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...
The Issue: A software error caused an increase in tray gripper motion errors that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence Recalled by...
The Issue: One lot of the Sofia 2 Flu + SARS Antigen FIA (Lot 709083) was labelled with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neurovascular embolization device. The Optima Coil System is a series...
The Issue: Discoloration was identified along the delivery pusher which was attributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for XR and 3.0T. Model (REF) Numbers 781270 Recalled by...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Prestige Coil System is a product family of embolic Recalled by BALT...
The Issue: Discoloration was identified along the delivery pusher which was attributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova. Model (REF) Numbers 781172. Recalled by Philips...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. HeartMate Touch Communication System Recalled by Thoratec Corp. Due to...
The Issue: Due to software and controller systems that results in unexpected pump start...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T. Model (REF) Numbers 781260 Recalled by...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX. Model (REF) Numbers 781271 Recalled by Philips North...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173. Recalled by...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion. Model (REF) Numbers 781346 Recalled by Philips...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.