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. 2,560 recalls have been distributed to Rhode Island in the last 12 months.
Showing 2241–2260 of 47,970 recalls
Recalled Item: Tirzepatide Injections Recalled by Thrive Health and Wellness, LLC, dba...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicotinamide adenine dinucleotide (NAD+): 100mg/mL Recalled by Thrive Health...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UNAVY ACIDO HIALURONICO Recalled by Umary-USA.com Due to Undeclared Ingredients
The Issue: Marketed without approved NDA/ANDA- Laboratory analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UMOVY ACIDO HIALURONICO Recalled by Umary-USA.com Due to Undeclared Ingredients
The Issue: Marketed without approved NDA/ANDA- Laboratory analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard Winged Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen...
The Issue: Due to a software/firmware issue diabetes management system may provide a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUCAS 2 Recalled by Jolife AB Due to Due to demonstration units of chest...
The Issue: Due to demonstration units of chest compression system being provided to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport HT70 Ventilator Recalled by Covidien Due to Ventilator Printed...
The Issue: Ventilator Printed Circuit Board Assembly may have two separate capacitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: My3D Personalized Solutions Humeral Cup Recalled by Onkos Surgical, Inc. Due...
The Issue: Required inspections were not performed on finished product prior to release...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC" MGIT" 960 PZA Kit. IVD qualitative procedure for Recalled by...
The Issue: BD has received additional complaints of intermittent false resistance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ColoSense Test Kit Recalled by Geneoscopy, Inc. Due to Multiple plate...
The Issue: Multiple plate failures documented as a result of the Low Positive Template...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ezetimibe and Simvastatin Tablets Recalled by Glenmark Pharmaceuticals Inc.,...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.