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. 2,510 recalls have been distributed to South Dakota in the last 12 months.
Showing 10761–10780 of 47,632 recalls
Recalled Item: Rifampin Capsules Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WEB Detachment Controller Recalled by MICROVENTION INC. Due to Detachment...
The Issue: Detachment controller, of an aneurysm embolization system, has an out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE CARDIOFORM ASD Occluder. cardiovascular implant. Recalled by W L Gore &...
The Issue: Due to manufacturing records (Release Test Results) indicating "Failed".
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride...
The Issue: Incorrect Product Formulation: Oxytocin 30 units was added to an IV bag of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 620G/ MMT-1750 MiniMed 640G/ MMT-1711 Recalled...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 630G/ MMT-1715 Recalled by Medtronic MiniMed Due...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MP Port Titanium Low Profile Implanted Port with 5F Recalled by...
The Issue: Printed Instructions for Use (IFU) not shipped with device. The Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has become aware of three potential software issues with ARTIS pheno...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonidine Hydrochloride Tablets Recalled by UNICHEM PHARMACEUTICALS USA INC...
The Issue: Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Indian Gooseberry Alcohol-Free Extract Recalled by Secrets Of The Tribe Due...
The Issue: Product has elevated level of lead.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amla Alcohol-Free Extract Recalled by Secrets Of The Tribe Due to Product...
The Issue: Product has elevated level of lead.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 Recalled by World...
The Issue: Dutch Red Potatoes were packed with a Dijon Mustard Sauce packet that did...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Atellica CH Lithium (Li) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neoral soft gelatin capsules (cyclosporine capsules Recalled by Novartis...
The Issue: CGMP deviations: Out of specification results obtained during routine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xolegel (ketoconazole) gel 2% Recalled by ALMIRALL, LLC Due to Failed...
The Issue: Failed Viscosity specification: Slightly higher OOS results obtained for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement...
The Issue: The product label claim for copper is 0.5mg, but third-party lab results...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: LVP software of the Ivenix Infusion System (IIS) Recalled by Fresenius Kabi...
The Issue: Retroactively reported correction from 2022: A software defect may cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prep-Fill Guarded Luer Connector (GLC): a. Part Number 57-400 Recalled by...
The Issue: Blister package had an unsealed edge compromising sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.