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. 2,386 recalls have been distributed to South Dakota in the last 12 months.
Showing 21341–21360 of 47,632 recalls
Recalled Item: GWB Special Flour Bulk Product Code 803011 Recalled by ADM - CHICAGO Due to...
The Issue: potential presence of E. coli. O26
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Latina Niagra Flour 50lbs bags Product Code 845202 Lot#: 8344BF Recalled by...
The Issue: potential presence of E. coli. O26
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ondansetron Injection Recalled by Fresenius Kabi USA, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROCHLORPERAZINE EDISYLATE INJECTION Recalled by Heritage Pharmaceuticals,...
The Issue: Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMIKACIN SULFATE INJECTION Recalled by Heritage Pharmaceuticals, Inc. Due to...
The Issue: Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Alinity ci-series System Control Modules which are configured with...
The Issue: All versions of the Alinity ci-series software may not detect an issue on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mosaic 310 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mosaic 310 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRG Salivary Testosterone ELISA- IVD for the detection of Testerone Recalled...
The Issue: Salivary assay may observe a higher percentage of samples with 0 pg/ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVivo EF app on Vscan Extend. Sold under the following Recalled by GE...
The Issue: Overestimation bias in automatically calculated ejection fraction (EF)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The device is a 25-gauge infusion line that is part Recalled by Dutch...
The Issue: Labeled 25-gauge surgical pack, TDC Vitrectomy Pack VGPC 25g, containing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guardian Connect App CSS7200 iOS and Guardian Connect Transmitter GST4C...
The Issue: Customers using the firm's continuous glucose monitoring system application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product...
The Issue: Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Visibly Online Vision Test which is part of Recalled by Opternative Inc...
The Issue: Lack of 510K clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86682003 Product...
The Issue: Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 60 ARTICULATING EXTRA THICK SULU Recalled by Covidien LLC Due to The...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.