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 5341–5360 of 47,970 recalls
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tivicay PD (dolutegravir) 5mg Tablets for Oral Suspension Recalled by...
The Issue: Labeling: Incorrect Lot and/or Expiration Date: The carton has incorrect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for...
The Issue: Potential for there to be a fluid ingress into the handle of the harvesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...
The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software version 5.3 in: RAPIDPoint 500e Blood Gas System (USA) Recalled by...
The Issue: Siemens Healthineers has identified an issue with the RAPIDPoint500e system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade Recalled...
The Issue: Cranial Caudal Blades manufactured incorrectly could result in fracture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...
The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...
The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System Recalled by...
The Issue: Potential for there to be a fluid ingress into the handle of the harvesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...
The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade Recalled...
The Issue: Cranial Caudal Blades manufactured incorrectly could result in fracture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RingLoc Bi-Polar Hip System Acetabular Cup Recalled by Biomet, Inc. Due to...
The Issue: 41 mm acetabular outer heads were potentially assembled with a 42 mm locking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim 5 Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim 7 Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TourniKwik Tourniquet Set (CFN 79012) Recalled by Medtronic Perfusion...
The Issue: Incorrect component placed in four manufactured lots of the TourniKwik"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim XR 5 Implantable Pulse Generator Recalled by Abbott Medical...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Liberta RC Recalled by Abbott Medical Due to Deep brain stimulation...
The Issue: Deep brain stimulation system will first turn off after approximately 50...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim 7 Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim XR 7 Implantable Pulse Generator Recalled by Abbott Medical...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.