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. 2,496 recalls have been distributed to Rhode Island in the last 12 months.
Showing 11521–11540 of 47,970 recalls
Recalled Item: GS DENTURE CLEANSER GRN TAB 40CT Recalled by Family Dollar Stores, Llc. Due...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B L BIOTRU MULTI PURPOSE SOLUTION 4 FLOZ Recalled by Family Dollar Stores,...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AT HOME MARIJUANA TEST STRIP Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SKYN ORIGINAL NON LATEX CONDOM 12CT Recalled by Family Dollar Stores, Llc....
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ Recalled by Family Dollar Stores, Llc....
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) CVS Health Sterile Surgical Pads Recalled by ASO LLC Due to The product...
The Issue: The product falls apart during handling after removal from its primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit...
The Issue: Due to preventative maintenance (PM) not being performed on E-100 generators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene Recalled by Meridian Bioscience Inc Due to When a run is aborted,...
The Issue: When a run is aborted, the cooling period protection does not occur and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CereLink ICP Monitor Recalled by Integra LifeSciences Corp. Due to Integra...
The Issue: Integra has received complaints associated with ICP readings drifting to -50...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Cholesterol- For the quantitative in vitro determination of...
The Issue: Product fails to meet the performance claims quoted on the kit insert:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules Recalled by SUN...
The Issue: Superpotent Drug: Out of specification for assay at the 12-month timepoint.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules Recalled by SUN...
The Issue: Superpotent Drug: Out of specification for assay at the 12-month timepoint.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...
The Issue: cGMP - Water leakage
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: etouchus Recalled by Touch US Llc Due to Device was marketed without FDA...
The Issue: Device was marketed without FDA 510(k) clearance or a PMA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit...
The Issue: BD Intraosseous Needle Kits may exhibit: 1) Increased force required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 50# (pound) Domino Light Brown Sugar. This is packaged in Recalled by Domino...
The Issue: Syrup used to manufacture Light Brown Sugar may have been exposed to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Daily Harvest French Lentil + leek Crumbles Recalled by DAILY HARVEST Due to...
The Issue: Product is linked to complaints of gastrointestinal illness.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Verigene CDF Nucleic Acid Test Recalled by Luminex Corporation Due to There...
The Issue: There is a potential for false negative results using VERIGENE CDF Stool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.