Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,341 recalls have been distributed to Rhode Island in the last 12 months.
Showing 33621–33640 of 47,970 recalls
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Bariatric Power Recliner Recalled by Hill-Rom, Inc. Due to The...
The Issue: The recliners were shipped without the foot rest ottoman linkage side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI H/S Cuvette Recalled by Sorin Group USA, Inc. Due to The CDI System 500...
The Issue: The CDI System 500 monitor displays the "H/S DISCONNECT AT CUVETTE" error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...
The Issue: Labeling: label error on declared strength.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...
The Issue: Labeling: label error on declared strength.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclopentolate Hydrochloride Ophthalmic Solution USP Recalled by Bausch &...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Tablets USP Recalled by Amerisource Health Services Due to...
The Issue: Failed Dissolution Specifications: Unexplained low out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: A Picture Archiving and Communication System (PACS) intended to display...
The Issue: To inform users about the possible incorrect values for Distance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics Due to Software Issue
The Issue: Software Issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile wDR motorized portable diagnostic X-ray systems. Intended for use...
The Issue: This is related to previous 806 Notifications about uncommanded movements of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Licorice Coughing Liquid (guaifenesin) Recalled by Master Herbs, Inc./Li Due...
The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared morphine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.