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. 2,521 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,521 in last 12 months

Showing 72817300 of 47,970 recalls

DrugOctober 23, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Phenytoin Oral Suspension Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed Content Uniformity Specifications

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 23, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules Recalled by Glenmark...

The Issue: Failed Impurities/Degradation Specifications:Out of Specification result...

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

Class III — Low RiskOngoing
Refund
DrugOctober 23, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Ranolazine Extended-Release Tablets 500mg Recalled by Glenmark...

The Issue: Failed Dissolution Specifications: Out of specification for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Ingenia 1.5T CX Recalled by Philips North America Llc Due to Potential...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Achieva 1.5T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Achieva 1.5T Initial System Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Intera 1.5T Power/Pulsar Recalled by Philips North America Llc Due to...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2023· Philips North America Llc

Recalled Item: Intera 1.5T Recalled by Philips North America Llc Due to Potential component...

The Issue: Potential component failure in the Gradient Coil could product smoke and/or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 20, 2023· Botanical Be

Recalled Item: Artri King con Origa y Omega 3 tablets Recalled by Botanical Be Due to...

The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 20, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Bisoprolol Fumarate and Hydrochlorothiazide Tablets Recalled by Glenmark...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugOctober 20, 2023· Botanical Be

Recalled Item: Reumo Flex caplets Recalled by Botanical Be Due to Undeclared Diclofenac

The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 20, 2023· Botanical Be

Recalled Item: Kuka Flex Forte caplets Recalled by Botanical Be Due to Undeclared Diclofenac

The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 20, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Deferasirox Tablets for Oral Suspension Recalled by Glenmark Pharmaceuticals...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2023· Zyla Life Sciences US Inc.

Recalled Item: Oxaydo (oxycodone HCl Recalled by Zyla Life Sciences US Inc. Due to...

The Issue: Sub-potent Drug: Lower potency than labeled.

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

Class III — Low RiskOngoing
Refund
DrugOctober 20, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Liothyronine Sodium Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...

The Issue: Failed Impurities/Degradation Specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Liothyronine Sodium Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...

The Issue: Failed Impurities/Degradation Specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2023· Edenbridge Pharmaceuticals, LLC

Recalled Item: Opium Tincture Recalled by Edenbridge Pharmaceuticals, LLC Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
FoodOctober 20, 2023· GIVE AND GO PREPARED FOODS CORP

Recalled Item: Item 19858 Recalled by GIVE AND GO PREPARED FOODS CORP Due to Potential...

The Issue: Potential plastic pieces in the product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund