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. 2,365 recalls have been distributed to South Dakota in the last 12 months.
Showing 23441–23460 of 47,632 recalls
Recalled Item: VITROS 5600 Integrated System-For use in the in vitro quantitative Recalled...
The Issue: Potential for the VITROS 5600 Integrated System to dispense an insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DX-D 600 Product Usage: The DX-D 600 system is a Recalled by Agfa N.V. Due...
The Issue: A supplier for the Agfa system noted a potential for the steel support...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Permobil powered wheelchairs Recalled by Permobil, Ab Due to This correction...
The Issue: This correction decision has been made because of a potential failure of one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...
The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...
The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Megestrol Acetate Oral Suspension Recalled by Mckesson Corporation Due to...
The Issue: Supterpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Institutional,...
The Issue: Failed Impurities/Degradation Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TECOTHERM NEO Recalled by Tec Com Gmbh Due to The action is being initiated...
The Issue: The action is being initiated due to potential installation of faulty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portable Suction Pump Recalled by Ohio Medical Corporation Due to The...
The Issue: The care-e-vac(R)3 Battery/AC Powered Portable Aspirator battery terminal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVS Aria Cage Recalled by Stryker Spine Due to The anterior and posterior...
The Issue: The anterior and posterior markers on the cage were on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK(R) 2 AST-P655 Recalled by bioMerieux, Inc. Due to Routine internal...
The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK(R) 2 AST-P640 Recalled by bioMerieux, Inc. Due to Routine internal...
The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IsoFlex LAL Support Surface Recalled by Stryker Medical Division of Stryker...
The Issue: Certain 2860 IsoFlex LAL support surfaces were assembled with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kit For...
The Issue: A deterioration of performance was identified with influenza type B Enzyme...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyclosporine 1% Human Eye Drops Recalled by Westlab Pharmacy, Inc. dba...
The Issue: Lack of Process Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADAA Cataract Drops Recalled by Westlab Pharmacy, Inc. dba Westlab Pharmacy...
The Issue: Lack of Process Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.