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.
Showing 1261–1280 of 47,970 recalls
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Option"ELITE Vena Cava Filter System UDI-DI code: 00886333217151 Recalled by...
The Issue: Due to complaints of increased resistance when advancing the dilator within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Workstation 5000 Recalled by Philips North America Due to Failure of...
The Issue: Failure of Environmental Stress Testing from a pinched power module wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product: STA Liatest D-Di Recalled by Diagnostica Stago, Inc. Due to A...
The Issue: A potential risk of underestimation of D-Dimer (D-Di) levels with the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Workstation 7000 Recalled by Philips North America Due to Failure of...
The Issue: Failure of Environmental Stress Testing from a pinched power module wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excelsior Medical Recalled by Medline Industries, LP Due to Medline has...
The Issue: Medline has identified a limited quantity of saline IV flush syringes that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iNSitu Bipolar Hip System Recalled by Theken Companies LLC Due to Downstream...
The Issue: Downstream recall for RES 97605, BioPro femoral components. Product failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 Recalled by Olympus Corporation...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60 Recalled by Olympus Corporation...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FERNO POWER X2 POWERED AMBULANCE COT Recalled by Ferno-Washington Inc Due to...
The Issue: The fastening post hardware could loosen allowing the fastening post to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TENACIO Pump without InhibiZone Recalled by Boston Scientific Corporation...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150 Recalled by Olympus Corporation of...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-1TH1100 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.