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. 2,349 recalls have been distributed to South Dakota in the last 12 months.
Showing 29721–29740 of 47,632 recalls
Recalled Item: TriForce Peripheral Crossing Set Recalled by Cook Inc. Due to Devices using...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Hemostasis Assembly Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Performer Introducer Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Performer Introducer Set Recalled by Cook Inc. Due to Devices...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Introducer Hausdorf-Lock Atrial Recalled by Cook Inc. Due to...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Radial Access Set Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHBG IMMULITE 2000/IMMULITE 2000 XPi For the in vitro diagnostic Recalled by...
The Issue: Certain lots of Sex Hormone Binding Globulin (SHBG) do not meet the thirty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 882480: BrightView designed for single or dual detector nuclear imaging...
The Issue: Four issues: 1. Motion controller problem stops scan and no data image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 882482: BrightView XCT 882454 BrightView X upgrade to XCT Recalled by...
The Issue: Four issues: 1. Motion controller problem stops scan and no data image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 882478: BrightView X designed for single or dual detector nuclear Recalled...
The Issue: Four issues: 1. Motion controller problem stops scan and no data image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norethindrone Acetate and Ethinyl Estradiol Tablets Recalled by Mylan...
The Issue: Chemical Contamination: out of specification results for impurities were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tarina Fe 1/20 (Norethindrone Acetate and Ethinyl Estradiol Tablets Recalled...
The Issue: Chemical Contamination: out of specification results for impurities were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glipizide extended-release tablets Recalled by Actavis Inc Due to Failed...
The Issue: Failed Dissolution Specifications. Above out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LipiFlow Thermal Pulsation System/LipiFlow Recalled by Tearscience, Inc Due...
The Issue: Labeling: The labeled storage temperature is not consistent with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iChemVELOCITY Urine Chemistry System Recalled by Beckman Coulter Inc. Due to...
The Issue: The probe misalignment or bending has the potential to lead to delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA Sample Diluent Recalled by Phadia US Inc Due to Erroneous EliA test...
The Issue: Erroneous EliA test results related to problems with liquid level detection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daavlin Aquex (DAAV1000) Recalled by Hidrex GmbH Due to The device was...
The Issue: The device was reclassified from a class III device to a class II device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hidrex USA DVP1000 Recalled by Hidrex GmbH Due to The device was...
The Issue: The device was reclassified from a class III device to a class II device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hidrex USA DP450 Recalled by Hidrex GmbH Due to The device was reclassified...
The Issue: The device was reclassified from a class III device to a class II device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buffered Lidocaine Recalled by Pharmedium Services, LLC Due to Labeling;...
The Issue: Labeling; Label Mixup; outer packaging is incorrectly labeled as Buffered...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.