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 45641–45660 of 47,632 recalls
Recalled Item: Lemon Hand Sanitizing Wipes [n-alkyl dimethyl benzyl ammonium chloride...
The Issue: CGMP Deviations: The products were manufactured with raw material which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fairytale Brand Peanut Butter Sprites Recalled by Fairytale Brownies, Inc...
The Issue: The firm initiated voluntarily recall because the products contains peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fairytale Brownies Brand Peanut Butter Brownies Recalled by Fairytale...
The Issue: The firm initiated voluntarily recall because the products contains peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fairytale Brownies Brand Peanut Butter Cookies Recalled by Fairytale...
The Issue: The firm initiated voluntarily recall because the products contains peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Late July Organic Mini Peanut Butter Sandwich Crackers packaged in Recalled...
The Issue: Organic Mini Peanut Butter Sandwich Crackers are recalled due to Sunland...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VENTANA (a member of the Roche Group) DISCOVERY ULTRA Recalled by Ventana...
The Issue: Potential for a waste fluid overflow condition to accur while running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENTANA (a member of the Roche Group) BenchMark ULTRA Recalled by Ventana...
The Issue: Potiential for a waste fluid overflow condition to accur while running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pro Time Microcoagulation System/ Pro Time 3 Cuvette Recalled by...
The Issue: Some Pro Time3 Test Cuvettes within a specified lot range may recover lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Philips Medical Systems...
The Issue: Philips is issued a Field Change Order to update Extended Brilliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE Parallel Walled Certain Implant Recalled by Biomet...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE 2 Tapered Certain Implant Recalled by Biomet 3i,...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes External Fixation System Tube to Tube Clamp Recalled by Synthes USA...
The Issue: The insert provided with the product for the specific lot number indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 PORT "OFF" MANIFOLD w/WASTE BAG Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical, Inc. has identified a potential comingling of components where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm Cancellous Bone Screw Intended to be used for the Recalled by Encore...
The Issue: A product complaint was received where a size 20 screw was labeled as size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CYANOCOBALAMIN INJECTION Recalled by Fresenius Kabi USA, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MIDAZOLAM HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ONDANSETRON INJECTION Recalled by Fresenius Kabi USA, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CellCept (mycophenolate mofetil) capsules Recalled by Genentech, Inc. Due to...
The Issue: Short Fill: some bottles contained less than 120-count per labeled claim.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Quetiapine Fumarate Tablets Recalled by Dr. Reddy's...
The Issue: Failed USP Dissolution Test Requirements: During analysis of long term...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Harry & David Creamy Caramel Peanut Spread Recalled by Harry and David...
The Issue: Product received from supplier is being recalled due to the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.