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.

47,970 total recalls
2,560 in last 12 months

Showing 10011020 of 13,384 recalls

DrugJune 10, 2024· Brands International Corporation

Recalled Item: Oatmeal Daily Moisturizing Body Lotion (1.3% Dimethicone) Recalled by Brands...

The Issue: Microbial Contamination of Non-Sterile Products: confirmed presence of mold...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2024· Homeocare Laboratories, Inc.

Recalled Item: STELLALIFE ADVANCED FORMULA Peppermint Recalled by Homeocare Laboratories,...

The Issue: Microbial Contamination of Non-Sterile Products: presence of Terribacillus...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2024· Homeocare Laboratories, Inc.

Recalled Item: STELLALIFE VEGA Oral Care Recalled by Homeocare Laboratories, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: multiple Bacillus species...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJune 4, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Amoxicillin and Clavulanate Potassium Tablets USP Recalled by Teva...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2024· Washington Homeopathic Products, Inc.

Recalled Item: Complete 30C/200C Homeopathic Kit Recalled by Washington Homeopathic...

The Issue: Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 30, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Cefixime for Oral Suspension USP 200 mg/5 mL (50 mL Pack size) Recalled by...

The Issue: Failed Content Uniformity Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2024· Consumer Product Partners, LLC

Recalled Item: Petroleum Jelly Recalled by Consumer Product Partners, LLC Due to Labeling:...

The Issue: Labeling: Label Mix up; product labeled as pure white petroleum jelly...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2024· Winder Laboratories, LLC

Recalled Item: Phenazopyridine HCl Tablets USP Recalled by Winder Laboratories, LLC Due to...

The Issue: Product Mix Up. A bottle of Phenazopyridine HCl tablets USP 100 mg contained...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2024· Sagent Pharmaceuticals

Recalled Item: Docetaxel Injection Recalled by Sagent Pharmaceuticals Due to Presence of...

The Issue: Presence of Particulate Matter: Presence of particulate matter from the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 28, 2024· Organon Llc

Recalled Item: Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container

The Issue: Defective Container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 28, 2024· Sagent Pharmaceuticals

Recalled Item: Docetaxel Injection Recalled by Sagent Pharmaceuticals Due to Presence of...

The Issue: Presence of Particulate Matter: Presence of particulate matter from the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 28, 2024· Organon Llc

Recalled Item: Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container

The Issue: Defective Container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 28, 2024· Organon Llc

Recalled Item: Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container

The Issue: Defective Container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 24, 2024· SYNCHRONICITY SPA INC, DBA SUNTE

Recalled Item: suntegrity Recalled by SYNCHRONICITY SPA INC, DBA SUNTE Due to CGMP Deviations

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2024· SYNCHRONICITY SPA INC, DBA SUNTE

Recalled Item: suntegrity Recalled by SYNCHRONICITY SPA INC, DBA SUNTE Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: Presence of Aspergillus...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 23, 2024· Eugia US LLC

Recalled Item: Dexamethasone Sodium Phosphate injection USP Recalled by Eugia US LLC Due to...

The Issue: Failed Impurities/Degradation Specifications: impurity sulfonic acid adduct...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund