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 71217140 of 47,970 recalls

DrugNovember 10, 2023· Golden State Medical Supply Inc.

Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2023· Golden State Medical Supply Inc.

Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2023· Fagron Compounding Services

Recalled Item: Tropicamide 1% (10mg/mL) Recalled by Fagron Compounding Services Due to...

The Issue: Labeling: Label Mix-Up: The label of a dropper bottle mistakenly states the...

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

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2023· Teva Pharmaceuticals USA, Inc

Recalled Item: Testosterone Gel Recalled by Teva Pharmaceuticals USA, Inc Due to OOS for...

The Issue: OOS for viscosity

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

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2023· Golden State Medical Supply Inc.

Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 6-7-8. indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 13.5-14.5-15.5. Indicated for endoscopic...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 6-7-8. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 18-19-20. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 8.5-9.5-10.5. indicated for endoscopic dilation...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 11-12-13. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 8.5-9.5-10.5. Indicated for endoscopic dilation...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 13.5-14.5-15.5. Indicated for endoscopic...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 18-19-20. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 11-12-13. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 16-17-18. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: 48IN (121.9CM) INJ LINE ROTATING ADAPT (900psi) Recalled by Smiths Medical...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: Medex 20IN (50.8CM) INJ LINE ROTATING ADAPT Recalled by Smiths Medical Asd...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: 1050 STOPCOCK LEFT ROTATOR OFF HANDLE Recalled by Smiths Medical Asd Inc Due...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing