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. 1,673 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
1,673 in last 12 months

Showing 4266142680 of 47,970 recalls

DrugSeptember 17, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: During stability testing an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: During stability testing an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Amgen, Inc.

Recalled Item: Prolia (denosumab) Injection Recalled by Amgen, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Visible cellulose fibers were observed in a...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 16, 2013· Hospira, Inc.

Recalled Item: Morphine Sulfate Injection Recalled by Hospira, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Confirmed customer report of leakage of vial...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 16, 2013· Osmotica Pharmaceutical Corp

Recalled Item: Venlafaxine (Venlafaxine Hydrochloride) extended release Tablets Recalled by...

The Issue: Failed Dissolution Specification:12 hour time point at 18 months of product...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 16, 2013· Hospira, Inc.

Recalled Item: 1% Lidocaine HCl Injection Recalled by Hospira, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Oxidized stainless steel found in vial of 1%...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Abbott Medical Optics, Inc.

Recalled Item: STAR Excimer Laser System Recalled by Abbott Medical Optics, Inc. Due to...

The Issue: This corrective action will address an identified failure of the lamp and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Abbott Medical Optics, Inc.

Recalled Item: STAR Excimer Laser System Recalled by Abbott Medical Optics, Inc. Due to...

The Issue: This corrective action will address an identified failure of the lamp and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Abbott Medical Optics, Inc.

Recalled Item: STAR ActiveTrak Excimer Laser System Recalled by Abbott Medical Optics, Inc....

The Issue: This corrective action will address an identified failure of the lamp and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Abbott Medical Optics, Inc.

Recalled Item: STAR Excimer Laser System with Variable Spot Scanning Recalled by Abbott...

The Issue: This corrective action will address an identified failure of the lamp and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences EMBOL-X Glide Protection System Recalled by Edwards...

The Issue: Edwards Lifesciences is recalling certain lots of EMBOL-X Glide Protection...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Pentax Medical Company

Recalled Item: PENTAX Endoscopic Accessories. OF-B194. Made in Japan. PENTAX Upper/Lower...

The Issue: PENTAX Medical has become aware of a product issue associated with the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing