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. 2,376 recalls have been distributed to Rhode Island in the last 12 months.
Showing 21221–21240 of 27,456 recalls
Recalled Item: Cannula and Seal Recalled by Stryker Sustainability Solutions Due to Stryker...
The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...
The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...
The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to Non-invasive...
The Issue: Non-invasive blood pressure pumps (NIBP) voltage is not sufficient and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 3100IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2100IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima IGS 320. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite M1000 in vitro diagnostic. Product Usage: The Tecan Infinite...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 3131IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 540. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite 200 in vitro diagnostic. Product Usage: The Tecan Infinite Recalled...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery IGS 740 & GE Healthcare Innova IGS Recalled by GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 520. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 620. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite 200 PRO in vitro diagnostic. Product Usage: The Tecan Recalled by...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2121IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.