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. 2,447 recalls have been distributed to South Dakota in the last 12 months.
Showing 16101–16120 of 47,632 recalls
Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ascend Laboratories Recalled by Ascend Laboratories LLC Due to Failed...
The Issue: Failed Impurity/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ascend Laboratories Recalled by Ascend Laboratories LLC Due to Failed...
The Issue: Failed Impurity/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esomeprazole Magnesium for Delayed-Release Oral Suspension 10mg Recalled by...
The Issue: Cross- contamination with other products: The excipient, Crospovidone, NF is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware...
The Issue: GE Healthcare has become aware of a potential issue on Revolution Apex,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware...
The Issue: GE Healthcare has become aware of a potential issue on Revolution Apex,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Medical Care NaturaLyte Liquid Acid concentrate-Liquid Acid...
The Issue: Bottles Missing Product Label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A calculator/data processing module for clinical use is an electronic...
The Issue: A software error results in the unintentional removal of the serum-indices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXOGEN Ultrasound Coupling Gel Recalled by Bioventus, LLC Due to Product may...
The Issue: Product may contain white particulates that are microbial in nature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Succinylcholine Chloride PF Inj. 200 mg/10 mL Recalled by US Compounding Inc...
The Issue: Labeling: Incorrect or Missing lot and/or expiration date: The lot number...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KWIK-STI(TM) Recalled by Microbiologics Inc Due to The expiration date on...
The Issue: The expiration date on the label of one component (negative control 0243U)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK 2 Pack Recalled by Microbiologics Inc Due to Contamination with S....
The Issue: Contamination with S. epidermidis
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...
The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...
The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...
The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Humidification Flask Recalled by Cook Medical Llc Due to A small...
The Issue: A small percentage of the Disposable Humidification Flasks may have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WAHL 4212 HEATED MASSAGER Recalled by Wahl Clipper Corp Due to The...
The Issue: The connection between the massager and heat element can overheat causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 Reperfusion Catheter The Penumbra JET Recalled by Penumbra...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7MAX KIT Penumbra JET 7 Reperfusion Catheter+ MAX Recalled by...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.