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. 2,512 recalls have been distributed to South Dakota in the last 12 months.
Showing 10001–10020 of 47,632 recalls
Recalled Item: Glycopyrrolate Tablets Recalled by AVKARE LLC Due to Failed...
The Issue: Failed impurities/degradation specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sanders Milk Chocolate Sea Salt Pecan Cluster: 0-35900-25550-2 .5OZ...
The Issue: Foreign material in product. Pieces of cleaning brush bristles found in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sanders Dark Chocolate Sea Salt Caramels: OZ Tub Recalled by Sanders Candy...
The Issue: Foreign material in product. Pieces of cleaning brush bristles found in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sanders Dark Chocolate Peppermint Sea Salt Caramel: OZ Recalled by Sanders...
The Issue: Foreign material in product. Pieces of cleaning brush bristles found in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sanders Dark Chocolate Maple Sea Salt Caramel: No oz. foil bag Recalled by...
The Issue: Foreign material in product. Pieces of cleaning brush bristles found in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sanders Assorted Milk and Dark Sea Salt Caramels Recalled by Sanders Candy...
The Issue: Foreign material in product. Pieces of cleaning brush bristles found in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sanders Milk Chocolate Sea Salt Caramels: OZ Tub Recalled by Sanders Candy...
The Issue: Foreign material in product. Pieces of cleaning brush bristles found in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short Recalled...
The Issue: Product Mislabeled on the outer bag and inner kit Tyvek header bag
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur XP and ADVIA Centaur XPT Anti-HBe2 (aHBe2) 50T- Recalled by...
The Issue: Anti-HBe2 (aHBe2) interference with the Hepatitis B e Antigen (HBeAg) Assay,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term...
The Issue: Label with the incorrect component listed on the inner kit Tyvek header bag
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Covera Vascular Covered Stent is a flexible Recalled by Bard Peripheral...
The Issue: An increase in the reported complaint rate for inability to deploy was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RipCord Syndesmosis Button Recalled by TriMed Inc. Due to Overly aggressive...
The Issue: Overly aggressive tension on the pull suture, while passing the medial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE UNITE FOOT & ANKLE DRILL BIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The recall is due to observed intra-operative screw failure. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE UNITE FOOT & ANKLE Screw Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The recall is due to observed intra-operative screw failure. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE UNITE FOOT & ANKLE Screw Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The recall is due to observed intra-operative screw failure. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Air-Q3 AirQ3 Standard ILA with Manual Cuff Inflation and GA Recalled by...
The Issue: There is an orogastric (OG) tube size discrepancy between the labeling in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge Flow-e Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Due to a software bug, under certain conditions, pressure cannot be built up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge Flow-c Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Due to a software bug, under certain conditions, pressure cannot be built up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge Flow-i Anesthesia Systems Flow-i C20 Recalled by Getinge Usa Sales...
The Issue: Due to a software bug, under certain conditions, pressure cannot be built up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software : myNeedle Guide 2D license Recalled by Siemens Medical Solutions...
The Issue: In the syngo.CT VA40 and syngo.CT VA50 myNeedle Guide application, the order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.