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 2181–2200 of 47,970 recalls
Recalled Item: Philips X5-1 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips S8-3t Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips XL14-3 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips C5-1 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips L12-4 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips VL13-5 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips L8-4 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips L9-3 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips S7-3t Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...
The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...
The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe...
The Issue: Due to an error in assembly of the thermistor within some units, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...
The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...
The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Long Nail Recalled by Stryker GmbH Due to Investigation confirmed that the...
The Issue: Investigation confirmed that the GAMMA4 Right Long Nail was manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion R1.x and R2.x systems Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: A software issue was identified in the internal communication process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Fresenius Medical Care Holdings,...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Tablets Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Tablets Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: O-arm O2 Imaging System. Mobile X-Ray System. Recalled by Medtronic...
The Issue: A mechanical component that supports the O2 gantry to the support structure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.