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. 2,363 recalls have been distributed to Rhode Island in the last 12 months.
Showing 23521–23540 of 27,456 recalls
Recalled Item: Merge Hemo software. Merge Hemo monitors Recalled by Merge Healthcare, Inc....
The Issue: The application may crash during the cath lab procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Robotic Arm Interactive Orthopedic System (RIO) Recalled by Mako Surgical...
The Issue: Revision of the field manual
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convatec Flexi Seal Control Fecal Management System Rx Only by Convatec Inc....
The Issue: Convatec Inc. is recalling Flexi-seal FMS Control Kit since it does not have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes ProDisc-C 2.0mm Milling Bit Recalled by Synthes, Inc. Due to Certain...
The Issue: Certain lots of the ProDisc-C 2.0mm Milling Bits have an increased potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems...
The Issue: Greatbatch identified that the documentation does not support the five-year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...
The Issue: Connection issues between the PD transfer set catheter connector and an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive...
The Issue: Serum albumin component monomer failed to meet internally established end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation software version 4.0.3.4 RayStation is a software system designed...
The Issue: This notice concerns a problem with the computation of ROI voxel volumes for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revision K Actuator Test Boards sold as replacement parts for Recalled by...
The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards...
The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oasis Coil Extension Cable used with Hitachi Oasis MRI System Recalled by...
The Issue: The firm received a complaint stating the Coil Extension Cable accessory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Amia Automated PD systems are used in the treatment Recalled by...
The Issue: System error 01779 is produced when the battery cannot be charged due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSTRUMENT TRACKER 9733533XOM ENT 1PK Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder Recalled by Davol,...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 4.5" Circle Reorder Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 8" Circle Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 6" CircleReorder Number: Recalled...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 6"x8" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mar Cor Purification Recalled by Mar Cor Purification Due to Mar Cor...
The Issue: Mar Cor Purification manufactured Central Water Plant (CWP) reverse osmosis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Composix" LIP Mesh with Echo PS" 8"x10" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.