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 9141–9160 of 27,456 recalls
Recalled Item: Scan Abutment SP Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment NP Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment WP Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment MU Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment SU Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Abutment PCA Recalled by Paltop Advanced Dental Solutions Ltd Due to...
The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci-series System Control Module clinical chemistry and immunoassay...
The Issue: Due to potential performance issues with software version 3.2.3 and earlier....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Recalled by Philips Respironics, Inc. Due to Two...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 Recalled by Philips Respironics, Inc. Due to Two software...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300 Recalled by Philips Respironics, Inc. Due to Two software...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Two software issues...
The Issue: Two software issues have been identified related to pressure increase in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norton Arm Kit Recalled by Aspen Surgical Products, Inc. Due to Affected...
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jessie Sterile Arm Suspension Kit Recalled by Aspen Surgical Products, Inc....
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marco Shoulder Stabilization Kit Recalled by Aspen Surgical Products, Inc....
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUGMENT Injectable Kit Recalled by BioMimetic Therapeutics, LLC Due to The...
The Issue: The kit contains the wrong vial tray in the package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraSphere Administration Set Recalled by Boston Scientific Corporation Due...
The Issue: Potential for leaks and loosening at the patient catheter connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraSphere Administration Set Recalled by Boston Scientific Corporation Due...
The Issue: Potential for leaks and loosening at the patient catheter connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter prismaflex Recalled by Baxter Healthcare Corporation Due to Products...
The Issue: Products labeled as sterile were distributed, but may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter PrismaFlex Recalled by Baxter Healthcare Corporation Due to Products...
The Issue: Products labeled as sterile were distributed, but may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD" Mouse IgG2a Isotype Control APC X39 ASR Recalled by Becton, Dickinson...
The Issue: Complaints have been received for performance issues related to high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.