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. 2,260 recalls have been distributed to South Dakota in the last 12 months.
Showing 44901–44920 of 47,632 recalls
Recalled Item: BUFFALO TRACE HOT BARBEQUE SAUCE Net Wt. 16 fl. oz./532 Recalled by Buffalo...
The Issue: The firm failed to include allergens of soy and anchovy on the labels of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BUFFALO TRACE ORIGINAL FLAVOR BARBEQUE SAUCE Net Wt. 16 fl. Recalled by...
The Issue: The firm failed to include allergens of soy and anchovy on the label of this...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...
The Issue: Observed instability of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of Malfunction S205 Backup Battery Failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of Malfunction S205 Backup Battery Failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineNet Anterior Cervical Cage Recalled by SpineNet Due to The recall...
The Issue: The recall decision has been made because because it has recently been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specialist 2 IM Rod Recalled by DePuy Orthopaedics, Inc. Due to Potential...
The Issue: Potential for the IM rod to break, leaving fragments in the patient....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended Release Tablets Recalled by American Health...
The Issue: Failed Stability Specifications; out of specification results at the 9 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benjamins Infants Gripe Mixture Recalled by Carib Import & Export, Inc. Due...
The Issue: CGMP Deviations: this product is being recalled because an FDA inspection...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SourceCF(R) Pediatric Drops Recalled by Aptalis Pharma Us Inc Due to The...
The Issue: The data suggests that the formulation does not support the shelf life of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to Symbiq Infusers...
The Issue: Symbiq Infusers have the potential to experience a white screen during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to Symbiq Infusers...
The Issue: Symbiq Infusers have the potential to experience a white screen during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to Frequent Proximal...
The Issue: Frequent Proximal Occlusion Alarms (POAs) occurring on Symbiq devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to Frequent Proximal...
The Issue: Frequent Proximal Occlusion Alarms (POAs) occurring on Symbiq devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Hospira Symbiq Infusion System is intended for the delivery of fluids...
The Issue: The devices secondary audio signal fails to activate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoGastric Solutions EsophyX2 Plus Device with Serosa Fastener and...
The Issue: EsophyX2Plus device was not validated under actual or simulated use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gen-Probe LIFECODES PF4 Enhanced assay Recalled by Genetic Testing...
The Issue: Lifecodes PF4 Enhanced assay, lot number 3000389, is being recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to Incorrect...
The Issue: Incorrect packaging of regular set and fast set cartridges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to Incorrect...
The Issue: Incorrect packaging of regular set and fast set cartridges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TEV-TROPIN (somatropin (rDNA origin) for injection) 5 mg (15 IU). Recalled...
The Issue: Labeling: Label Mix-up: Units of Lot 201131320087 are packaged in cartons...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.