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. 2,276 recalls have been distributed to Rhode Island in the last 12 months.
Showing 41981–42000 of 47,970 recalls
Recalled Item: Atrium Ocean Water Seal Chest Drain ATS (Autotransfusion) Blood Recovery...
The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution CR Articular Surface Provisional-Striped Green...
The Issue: This is an expansion of the June 2013 recall of NexGen Micro components....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Asante Conset Infusion Set with 60cm tubing & 9mm cannula packaged in...
The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery...
The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Ocean Water Seal Chest Drain ATS Blood Recovery System Recalled by...
The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NATURECT Capsules Dietary Supplement 500 mg Recalled by Tendex Due to...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: vitaliKOR Ready When You Are Recalled by Vitality Research Labs LLC Due to...
The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: P-BOOST Capsules Dietary Supplement 500 mg Recalled by Tendex Due to...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 50 mg Nitroglycerin in 5% Dextrose Injection (200 mcg/mL) Recalled by Baxter...
The Issue: Presence of Particulate Matter; particulate matter in one vial identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETOCONAZOLE CREAM Recalled by Fougera Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification degradant...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RezzRX capsules Recalled by Fossil Fuel Products, LLC Due to Undeclared...
The Issue: Marketed Without an Approved NDA/ANDA: Fossil Fuel Products, is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clinimix 5/15 sulfite-free (5% Amino Acid in 15% Dextrose) Injection...
The Issue: Presence of Particulate Matter: Particulate matter includes wood, sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in...
The Issue: Presence of Particulate Matter: Particulate matter includes wood, sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clinimix 4.25/25 sulfite-free (4.25% Amino Acid in 25% Dextrose) Injection...
The Issue: Presence of Particulate Matter: Particulate matter includes wood, sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 4-7 HP Recalled by...
The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED Size 4-7 Recalled by...
The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 2-3 HP Recalled by...
The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Delta Shunt Assembly Kit with Bioglide Small Recalled by Medtronic...
The Issue: Medtronic Neurosurgery is recalling the CSF-Unitized Shunts, Delta Shunt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 4-7 Recalled...
The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 4-7 HP Recalled by...
The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.