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. 2,539 recalls have been distributed to Rhode Island in the last 12 months.
Showing 5261–5280 of 27,456 recalls
Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 250-Intended for...
The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 400-Intended for...
The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 750-Intended for...
The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) Recalled by...
The Issue: Use of a 1.4 drill in hard bone conditions caused increased insertion forces...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD11b APC: ASR Recalled by Becton, Dickinson and Company, BD Biosciences Due...
The Issue: In vitro diagnostics product that impacts the quality of cell staining can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products ECO2 Slides-For in vitro diagnostic use only....
The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed during routine testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INDICAID COVID-19 Rapid Antigen At-Home Test Recalled by PHASE SCIENTIFIC...
The Issue: COVID-19 rapid antigen at home tests were released with an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRAPHENANO DENTAL G-CAM Recalled by GRAPHENANO DENTAL SL Due to Machining...
The Issue: Machining error on cams renders the device unusable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Select Cycler Recalled by Fresenius Medical Care Holdings, Inc. Due...
The Issue: Affected Liberty Select cyclers may display an incorrect time stamp on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Initial System Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by Philips North America Llc Due to Potential component...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Power/Pulsar Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX Recalled by Philips North America Llc Due to Potential...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit -For access to the subarachnoid space Recalled by...
The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Processing Module The Alinity i Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combo Kit Consists OF 10-110/INS-4500/INS-7040- For access to the...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.