Product Recalls in South Dakota
Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,516 recalls have been distributed to South Dakota in the last 12 months.
Showing 9201–9220 of 27,558 recalls
Recalled Item: Status COVID-19/Flu Rapid Immunoassay for Direct Detection and Differential...
The Issue: Products may have been distributed to customers other than laboratories...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma)...
The Issue: Products may have been distributed to customers other than laboratories...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of...
The Issue: Products may have been distributed to customers other than laboratories...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.