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 24041–24060 of 27,456 recalls
Recalled Item: 23ga Wide Field Corona Endo Illuminator Recalled by Synergetics Inc Due to...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25ga Wide Field Corona Endo Illuminator Recalled by Synergetics Inc Due to...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Standard tubing set Recalled by Synergetics Inc Due to Faulty seals on the...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23ga Endo Illuminator (Eckardt Trocar Compatible) Recalled by Synergetics...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "The Corona" Shielded Wide Field Endo Illuminator Recalled by Synergetics...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23ga Straight Fixed Extended Illuminated Laser Probe Recalled by Synergetics...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25ga Awh Chandelier Recalled by Synergetics Inc Due to Faulty seals on the...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid (tm) Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrocare SPORTS MEDICINE Recalled by ArthroCare Medical Corporation Due to...
The Issue: A sharp edge on the cannulated tip of the device may damage or cut a suture.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25ga Mid-Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25ga Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals on the...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Blood Set Recalled by Gambro Renal Products, Incorporated...
The Issue: Occluded heparin tubing events preventing anticoagulation dosing on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25ga Awh Chandelier Recalled by Synergetics Inc Due to Faulty seals on the...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)...
The Issue: The housing to the Pump's driveline connector became partially or fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium Single Lumen Low-Profile port Recalled by Bard Access Systems Due...
The Issue: Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRI Low Profile Single Lumen port with Open-Ended 6.6Fr Silicone Recalled by...
The Issue: Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estrogen Receptor AB-11 (Clone ID5) Mouse Monoclonal Antibody 1 mk Recalled...
The Issue: Reports that the product is not performing as expected. In house testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catheter Recalled by Merit Medical Systems, Inc. Due to Merit Medical...
The Issue: Merit Medical Systems, Inc. is conducting a recall for 3 lots of Maestro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Essenta DR Recalled by Philips Medical Systems, Inc. Due to X-ray...
The Issue: X-ray system C-arm casting may loosen and fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symmetry and CODMAN brands Recalled by Symmetry Medical/SSI Due to The...
The Issue: The Quad-Lock Sterilization Container System may not maintain an effective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.