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. 2,442 recalls have been distributed to South Dakota in the last 12 months.
Showing 16641–16660 of 47,632 recalls
Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...
The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...
The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil and Hydrochlorothiazide Tablets Recalled by Mylan...
The Issue: Out-of-specification organic impurity results obtained during routine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinnamon Apple Crisps packaged under the following Brands and sizes:...
The Issue: Product may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's Hatch Valley Salsa Recalled by Desert Premium Group, LLC Due to...
The Issue: One batch of salsa had a recorded equilibrium pH of 6.65.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...
The Issue: Potential contamination with S. epidermidis E. coli and S. warneri.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Recalled by...
The Issue: Potential contamination with Escherichia coli Staphylococcus epidermidis and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO DISK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...
The Issue: Potential contamination with Escherichia coli, Staphylococcus epidermidis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Conquest PTA Balloon dilation Catheter Recalled by Bard Peripheral...
The Issue: Dilation catheter packaged with the wrong size balloon. The labeling states...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Immunodiagnostic Products Anti-SARS-CoV-2 IgG Control - Product...
The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products-SARS-CoV-2 IgG Calibrator - Product Usage:...
The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COAPTITE Injectable Implant Recalled by Merz North America, Inc. Due to The...
The Issue: The Instructions for Use (IFU) updated 03/02/2020 does not match data listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Monitoring Unit (BMU 40) Recalled by Maquet Cardiovascular Us Sales,...
The Issue: The Printed Circuit Board Assembly (PCBA) are not in compliance with the IEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BladderScan Prime Plus Probe - Product Usage: intended Recalled by Verathon,...
The Issue: Due to a change in handle material and process, probe handle may crack.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluocinonide Ointment USP 0.05% Recalled by Teligent Pharma, Inc. Due to...
The Issue: Failed Impurities/Degradation - Out-of-specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AB PowerCel 170 (velvet black) Recalled by Advanced Bionics, LLC Due to...
The Issue: Mislabeling; It has been determined that some batteries were improperly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB PowerCel 230 (velvet black) Recalled by Advanced Bionics, LLC Due to...
The Issue: Mislabeling; It has been determined that some batteries were improperly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Happy Ducts Compress Recalled by Wishgarden Herbs, Incorporated Due to...
The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Goldenseal POWDER Recalled by Wishgarden Herbs, Incorporated Due to...
The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cord Care POWDER Recalled by Wishgarden Herbs, Incorporated Due to Microbial...
The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.