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. 2,368 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,368 in last 12 months

Showing 2348123500 of 47,970 recalls

DrugSeptember 4, 2018· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Synjardy (empagliflozin and metformin hydrochloride) Tablets. 5 mg/1000 mg....

The Issue: Cross Contamination With Other Products:

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Tizanidine HCl Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Presence of Foreign Tablets/Capsules: Glimepiride tablet was found in a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Skin Irritation & Itch Response Homeopathic Formula Recalled by Beaumont...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Muscle & Joint Pain Relief Homeopathic Formula Recalled by Beaumont Bio-med,...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Arthritis Pain Relief Homeopathic Formula Recalled by Beaumont Bio-med, Inc....

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Colds & Flu Response Homeopathic Formula Recalled by Beaumont Bio-med, Inc....

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· BioLyte Laboratories, LLC

Recalled Item: NeoRelief for Muscle Cramping & Restlessness Homeopathic Topical Gel...

The Issue: CGMP Deviations: finished product produced with active ingredients recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Sinus Response Homeopathic Formula Recalled by Beaumont Bio-med, Inc. Due to...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Allergy & Hay Fever Relief Homeopathic Formula Recalled by Beaumont Bio-med,...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Diarrhea Response Homeopathic Formula Recalled by Beaumont Bio-med, Inc. Due...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Sore Throat & Laryngitis Response Homeopathic Formula Recalled by Beaumont...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 31, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: VirtuoSaph Plus Endoscopic Vessel Harvesting System Recalled by Terumo...

The Issue: The system's IFU contains a list of generators that the have been deemed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2018· Accuray Incorporated

Recalled Item: Ashland(TM) Box Film Ball Cube II EBT3 Recalled by Accuray Incorporated Due...

The Issue: the Ball Cube II phantom calibration film was not manufactured within...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2018· GE Healthcare, LLC

Recalled Item: Solar 8000i Patient Monitoring System is used to monitor physiologic...

The Issue: The patient monitors may simultaneously restart as designed if all are...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2018· GE Healthcare, LLC

Recalled Item: Dash 4000 Patient Monitoring System is used to monitor physiologic Recalled...

The Issue: The patient monitors may simultaneously restart as designed if all are...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2018· GE Healthcare, LLC

Recalled Item: Dash 3000 Patient Monitoring System is used to monitor physiologic Recalled...

The Issue: The patient monitors may simultaneously restart as designed if all are...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2018· GE Healthcare, LLC

Recalled Item: Solar 8000M Patient Monitoring System is used to monitor physiologic...

The Issue: The patient monitors may simultaneously restart as designed if all are...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2018· GE Healthcare, LLC

Recalled Item: Solar 9500 Information Monitoring System is used to monitor physiologic...

The Issue: The patient monitors may simultaneously restart as designed if all are...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2018· GE Healthcare, LLC

Recalled Item: Dash 5000 Patient Monitoring System is used to monitor physiologic Recalled...

The Issue: The patient monitors may simultaneously restart as designed if all are...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2018· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Mitek Screw and Washer Depth Gauge Recalled by DePuy Mitek, Inc., a Johnson...

The Issue: The device has an offset in the design that results in a reading...

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

Class II — Potential Health HazardOngoing