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. 2,631 recalls have been distributed to Massachusetts in the last 12 months.
Showing 18421–18440 of 52,647 recalls
Recalled Item: RIOMET ER (metformin hydrochloride for extended-release oral suspension)...
The Issue: CGMP Deviations: Detection of N-nitrosodimethylamine (NDMA) impurity in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WILD MUSHROOM BARLEY soup Recalled by Hale And Hearty Soups, LLC Due to...
The Issue: Product may contain pieces of maggots.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ProVu Single Use Video Stylet with ET Tube Recalled by Flexicare Medical...
The Issue: When the video stylet cuff is over-inflated there is potential for occlusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kangaroo Connect 1000ml Bag Set Recalled by Cardinal Health 200, LLC Due to...
The Issue: The feeding spike sets may leak at the interface of the tube and spike...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kangaroo Connect 500ml Bag Set Recalled by Cardinal Health 200, LLC Due to...
The Issue: The feeding spike sets may leak at the interface of the tube and spike...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TroClose 1200 - Product Usage: intended for use in a variety of gynecologic...
The Issue: Endotoxin test results found above the acceptable levels in LAL test (above...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9372HD Digital Capture (ver. 1.1.0 + w/ 9263 endoPortal) Recalled by Pentax...
The Issue: There is an intermittent software issue that could affect the systems, in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visual-ICE MRI Cryoablation System Mobile Connection Panel (Visual-ICE MRI...
The Issue: Incorrectly installed base.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9310HD Digital Video Capture Module with software version 3.4.0 or Recalled...
The Issue: There is an intermittent software issue that could affect the systems, in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shirakiku brand Black Fungus (Kikurage) Recalled by Wismettac Asian Foods,...
The Issue: California Department of Public Health sampled and tested Shirakiku brand...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Revolution Apex Recalled by GE Healthcare, LLC Due to There is a potential...
The Issue: There is a potential for a smudge artifact that could be suspect for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray...
The Issue: Potential malfunction in which the examination room monitor may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo XP ProVue Retriever Recalled by Stryker Neurovascular Due to Increase...
The Issue: Increase in fracture complaints of the flexible, tapered core wire,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis (GII) - Product Usage: designed for use in patients Recalled by...
The Issue: The anterior locking detail does not meet its design specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Icono Interventional Fluoroscopic X-Ray system - Product Usage:...
The Issue: There is a software problem which affects the DSA Roadmap application on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NP Thyroid 15 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: FDA analysis found these products to be less than the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NP Thyroid 120 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent...
The Issue: Subpotent Drug: FDA analysis found these products to be less than the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A Li-Gator Single Use Laparoscopic Clip Applier Recalled by Genicon, Inc....
The Issue: Device malfunction causing the applier to jam, and clip loading failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Recalled...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.