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. 1,037 recalls have been distributed to Rhode Island in the last 12 months.
Showing 14461–14480 of 47,970 recalls
Recalled Item: Adenosine Injection Recalled by Teva Pharmaceuticals USA Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vecuronium Bromide for Injection 10 mg Recalled by Teva Pharmaceuticals USA...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclobenzaprine Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA...
The Issue: CGMP Deviations: Out of specification (OOS) test result for Total Aerobic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclobenzaprine Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA...
The Issue: CGMP Deviations: Out of specification (OOS) test result for Total Aerobic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Ointment USP Recalled by Teligent Pharma, Inc. Due to Failed...
The Issue: Failed Viscosity Specifications: lot does not meet specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Erythromycin Topical Solution USP Recalled by Teligent Pharma, Inc. Due to...
The Issue: Defective container: possibility for lack of seal integrity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclobenzaprine Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA...
The Issue: CGMP Deviations: Out of specification (OOS) test result for Total Aerobic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epoprostenol Sodium for Injection Recalled by Teva Pharmaceuticals USA Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DAUNOrubicin Hydrochloride Injection 20 mg/4mL Recalled by Teva...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HANA/PROFx CLASSIC FEMORAL HOOK RIGHT Recalled by Mizuho OSI Due to One...
The Issue: One batch of "regular" femoral hooks were incorrectly etched with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit ( by Sentinel CH...
The Issue: Calibrator vials were incorrectly labeled. Use of incorrectly labeled vials...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYMOL Medical Elite X Class Rigid Bronchoscope System Recalled by Lymol...
The Issue: Reprocessing instructions were revised November 15, 2020, to new processes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OASIS MRI System Recalled by Hitachi Healthcare Americas Corporation Due to...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON MRI System Recalled by Hitachi Healthcare Americas Corporation Due...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON Oval MRI System Recalled by Hitachi Healthcare Americas Corporation...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee Patella Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee CS Insert Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin TriFit TS Recalled by Corin Ltd Due to The packaging system on the...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee Augments Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Performa Test Strip Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Test strip vials may open while inside sealed cartons during shipment. An...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.