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. 2,311 recalls have been distributed to South Dakota in the last 12 months.
Showing 37101–37120 of 47,632 recalls
Recalled Item: Raisin Nut Party Mix: Aurora Recalled by Aurora Products, Inc. Due to...
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Deluxe Mixed Nuts with Sea Salt: Aurora Recalled by Aurora Products, Inc....
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roasted Mixed Nuts No Salt: Gourmet Garage Recalled by Aurora Products, Inc....
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Carter-Thomason II Port Closure System Recalled by CooperSurgical, Inc. Due...
The Issue: The pad printing around the suture entry holes on the 15mm Suture Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: Deterioration in performance of the Liquid Stable (LS) 2-Part HOMOCYSTEINE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMARTABLATE RF Generator System Recalled by Biosense Webster, Inc. Due to...
The Issue: Biosense Webster is recalling the SMARTABLATE Generator System because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q/ Q zen systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: potential issue with the Artis Q/ Q zen systems where it is possible that an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOW PROFILE NON-LOCK SCREW Recalled by Biomet, Inc. Due to A Biomet...
The Issue: A Biomet investigation found that the Low Profile Non-Locking Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARBOplatin Injection 450 mg/45 mL (10 mg/mL) Recalled by Mylan...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methotrexate Injection Recalled by Mylan Institutional LLC Due to Presence...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....
The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....
The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....
The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kraft Macaroni & Cheese Boxed Dinner Original Flavor Recalled by Kraft Foods...
The Issue: This voluntary recall has been initiated because Kraft Macaroni & Cheese...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's Nuts Raw California Walnut Pieces NET WT. 16oz. Recalled by...
The Issue: The firm is recalling Raw Walnuts because the products have the potential to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic Dual Chamber Temporary External Pacemaker Recalled by Medtronic...
The Issue: Possible performance issue when used with specific AA-sized (LR6) batteries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD99 Catalog number PM008 AA Recalled by Biocare Medical, LLC Due to A drop...
The Issue: A drop in staining intensity over time has been observed. These lots may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Monopty Disposable Core Biopsy Instruments and Kits Recalled by Bard...
The Issue: Bard Peripheral Vascular is recalling the Bard Monopty Disposable Core...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.