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. 2,521 recalls have been distributed to Rhode Island in the last 12 months.
Showing 8201–8220 of 47,970 recalls
Recalled Item: Alcon Custom Pak Recalled by Alcon Research, LTD. Due to Reports of patient...
The Issue: Reports of patient injury during use in procedures due to potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter Recalled by Covidien LP...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phaco Standalone Tips Recalled by Alcon Research, LTD. Due to Reports of...
The Issue: Reports of patient injury during use in procedures due to potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROBAT SUV Vacuum Off-Pump System Recalled by Maquet Cardiovascular, LLC...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCESSRAIL Platform (Standard Blade) Part Number SB-1000 Recalled by Maquet...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROBAT-i Vacuum Stabilizer System Recalled by Maquet Cardiovascular, LLC...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROBAT V Vacuum Off-Pump System Recalled by Maquet Cardiovascular, LLC Due...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Albuterol Sulfate Inhalation Aerosol Recalled by Cipla USA, Inc. Due to...
The Issue: Defective container: empty inhaler and leakage observed through the inhaler...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Strides Pharma Inc. Due to Presence...
The Issue: Presence of Foreign Substance: Presence of a small piece of blue plastic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tizanidine Hydrochloride Tablet 4mg Recalled by Preferred Pharmaceuticals,...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ISee Ortho-K Lens Recalled by PARAGON VISION SCIENCES, Inc Due to...
The Issue: Manufactured lenses are not covered by existing FDA approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fargo Ortho-K Lens Recalled by PARAGON VISION SCIENCES, Inc Due to...
The Issue: Manufactured lenses are not covered by existing FDA approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.