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. 2,539 recalls have been distributed to Rhode Island in the last 12 months.
Showing 5041–5060 of 13,384 recalls
Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Zantac 150 mg Distributed by: Chattem Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cool Mint Maximum Strength Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 150 mg Distributed by: Chattem Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol Vaginal Inserts USP Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: Defective Delivery System: complaints for difficulty in pushing the plunger...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Succinylcholine Chloride Injection Recalled by Nephron Pharmaceuticals...
The Issue: Incorrect labeling: Incorrect or missing lot and/or exp date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prasugrel Tablets 5 mg Recalled by Mylan Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Dissolution Specification: Low out of specification dissolution results.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bimatoprost Ophthalmic Solution 0.03% Recalled by Sandoz Inc Due to...
The Issue: Labeling: Incorrect or missing package insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gatifloxacin Ophthalmic Solution 0.5% Recalled by Sandoz Inc Due to...
The Issue: Labeling: Incorrect or missing package insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension...
The Issue: Labeling: Incorrect or missing package insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Prolo Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Relief + Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-MuSkel-Neural Recalled by 8046255 Canada Inc. DBA Viatrexx Due to...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Articula Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Infla Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.