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 23381–23400 of 47,632 recalls
Recalled Item: Beckman Coulter Uric Acid Recalled by Beckman Coulter Inc. Due to NAPQI, a...
The Issue: NAPQI, a metabolite of Acetominophen, causes negative interference with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyroid Powder Recalled by LGM Pharma LLC Due to CGMP Deviations: Thyroid...
The Issue: CGMP Deviations: Thyroid Powder has inconsistent levels of the active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethosuximide Capsules Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Compulsin Recalled by Hellolife Due to Microbial Contamination of Non...
The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neuroveen Recalled by Hellolife Due to Microbial Contamination of Non...
The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Respitrol Recalled by Hellolife Due to Microbial Contamination of Non...
The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Children s Advil Suspension Ibuprofen Oral Suspension Recalled by Pfizer...
The Issue: Labeling Error: Not elsewhere classified. product has a dosage cup marked in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyroveev Recalled by Hellolife Due to Microbial Contamination of Non...
The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Extended-Release Tablets Recalled by LUPIN SOMERSET Due to...
The Issue: Failed Impurities/Degradation Specifications: Morphine Sulfate Extended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AIA-360 Analyzer Recalled by Tosoh Bioscience Inc Due to The firm has...
The Issue: The firm has implemented new product labeling changes for the Tosoh AIA-360...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva...
The Issue: One lot of the specified needles is not performing as intended due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp Recalled...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp :...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 12mm SpinDown Clamp Recalled by Zimmer...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco(R) ViaValve(TM) safety intravenous (I.V.) catheters Recalled by Smiths...
The Issue: Several lots of Jelco¿ ViaValve" safety intravenous (I.V.) catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp :...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp Recalled...
The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.