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. 1,663 recalls have been distributed to South Dakota in the last 12 months.
Showing 43041–43060 of 47,632 recalls
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL Recalled by Ecolab...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pyridostigmine Bromide Tablets 60 mg Recalled by Core Pharma Llc Due to...
The Issue: Failed Stability Specifications: Pyridostigmine Bromide tablets, is being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benztropine Mesylate Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of particulate matter: characterized as thin colorless flakes that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RemB Electric Universal Driver For use with the Recalled by Stryker...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRidium 1145 Dose Reduction System (DERS) drug library kit. (This Recalled...
The Issue: The Dose Error Reduction System (DERS) can indicate an incorrect recommended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker TPS Universal Driver 99 Rx Recalled by Stryker Instruments Div. of...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE Universal Driver 99 Rx Only This drill Recalled by Stryker Instruments...
The Issue: The safety margin values detailed in the Engineering Design were entered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Tacrolimus Flex reagent cartridge (DF107) and Dimension TACR CAL...
The Issue: Siemens initiated a recall due to confirmed complaints of low patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico Recalled by...
The Issue: The firm initiated this recall of certain lots of Illico Ti Cannulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Preimplantation Test Kit Recalled by Medtronic Neurosurgery Due to...
The Issue: Medtronic Neurosurgery is recalling the Medtronic Preimplantation Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...
The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Calibrator A. Cat. #04800735 Recalled by Siemens Healthcare...
The Issue: Calibrator A lot CA77 is under-recovering to the assigned target for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...
The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NataChew Recalled by Stayma Consulting Service, LLC. Due to Subpotent; Beta...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA 430 ec Recalled by Stayma Consulting Service, LLC. Due to...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA 430 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA 400 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA Balanced Recalled by Stayma Consulting Service, LLC. Due to...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duet DHA 400 ec Recalled by Stayma Consulting Service, LLC. Due to...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nata Komplete Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...
The Issue: Subpotent; Beta carotene (Vitamin A)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.