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 5161–5180 of 27,456 recalls
Recalled Item: Guardian 4 Glucose Sensor Recalled by Medtronic MiniMed, Inc. Due to Some...
The Issue: Some sensors may have a glucose oxidase (GOX) layer thickness outside of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoClean 2 Recalled by SoClean, Inc Due to New User Manual with additional...
The Issue: New User Manual with additional instructions for use and a hose and mask...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoClean 3 Recalled by SoClean, Inc Due to New User Manual with additional...
The Issue: New User Manual with additional instructions for use and a hose and mask...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Amia Automated Peritoneal Dialysis (APD) Cycler Set Recalled by...
The Issue: There is to an increase in complaints related to failure alarms for Wet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensica Urine Output System Recalled by C.R. Bard Inc Due to BD (C.R. Bard)...
The Issue: BD (C.R. Bard) has received user complaints reporting that when the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX Spectranetics...
The Issue: Incorrect product labeling. Exterior product box label does not match...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOHELP-i Heart Lung Support System: Blood oxygenation and carbon dioxide...
The Issue: CARDIOHELP-i System was not properly tested to measure leakage current
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous probe connection cable ( and 701048804) used with Recalled by Maquet...
The Issue: Firm received complaints of breaks in the insulation, shielding, or wires of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS...
The Issue: Identification label on affected hookups could become illegible over time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibration Serum Level 3. CAL 3 Recalled by Randox Laboratories Ltd. Due to...
The Issue: There have been transcription errors on the Instructions For Use (IFU) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORI REAL INTELLIGENCE Robotic Drill Recalled by Blue Belt Technologies, Inc...
The Issue: Possibility that the user is unable to resolve drill disconnection error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 18-19-20. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 13.5-14.5-15.5. Indicated for endoscopic...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 18-19-20. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 13.5-14.5-15.5. Indicated for endoscopic...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 16-17-18. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 11-12-13. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 6-7-8. indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO surgical EMPOWR Porous Knee System Empowr 3D Femur-Porous Coated...
The Issue: Due to incorrect product/device within packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.