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. 2,534 recalls have been distributed to South Dakota in the last 12 months.
Showing 5221–5240 of 47,632 recalls
Recalled Item: OMTech Desktop Laser Engraver Recalled by Rygel Advanced Machines d/b/a...
The Issue: Lack of redundant interlocks, missing required labels and certification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STELLALIFE ADVANCED FORMULA Peppermint Recalled by Homeocare Laboratories,...
The Issue: Microbial Contamination of Non-Sterile Products: presence of Terribacillus...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STELLALIFE VEGA Oral Care Recalled by Homeocare Laboratories, Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products: multiple Bacillus species...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...
The Issue: There are two software bug issues with the analyzer. Issue 1: When a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE XL TORSO COIL 1.5T. 16-element receive only coil for Recalled by...
The Issue: Potential for coils to heat up and harm patients (burn).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE XL TORSO COIL 3.0T. 16-element receive only coil for Recalled by...
The Issue: Potential for coils to heat up and harm patients (burn).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil Recalled by...
The Issue: Potential for coils to heat up and harm patients (burn).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amoxicillin and Clavulanate Potassium Tablets USP Recalled by Teva...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dxl 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: The analyzers were built with nonconforming USB cables made with brass...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyno Medical Z800 Recalled by Zyno Medical LLC Due to Zyno Medical has found...
The Issue: Zyno Medical has found that certain Z800, Z800F, Z800W, and Z800WF pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bag Decanter II Recalled by Microtek Medical Inc. Due to During sterile...
The Issue: During sterile barrier testing performed on the decanter product line, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vial Decanter Recalled by Microtek Medical Inc. Due to During sterile...
The Issue: During sterile barrier testing performed on the decanter product line, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bottle Decanter Recalled by Microtek Medical Inc. Due to During sterile...
The Issue: During sterile barrier testing performed on the decanter product line, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Flow Bag Decanter Recalled by Microtek Medical Inc. Due to During sterile...
The Issue: During sterile barrier testing performed on the decanter product line, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transfer Device Recalled by Microtek Medical Inc. Due to During sterile...
The Issue: During sterile barrier testing performed on the decanter product line, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAcube Connect MDx - IVD Instrument designed to perform automated Recalled...
The Issue: Heater shaker module does not perform heating if the temperature is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTL190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings,...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTLR190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings,...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 190904 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare part...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings, Inc....
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.