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. 2,339 recalls have been distributed to South Dakota in the last 12 months.
Showing 33001–33020 of 47,632 recalls
Recalled Item: Laparotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to These...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MEDICAL AngioVac Circuit Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-18 360 11MM X 30CM Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Latex Free Recalled by Windstone Medical Packaging, Inc. Due...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiCounter scanner Recalled by Stryker Instruments Div. of Stryker...
The Issue: The affected scanner does not correctly interact with the SC360 software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded Recalled by Becton...
The Issue: The device may have a defect in the catheter. In some instances this defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System...
The Issue: Mislabeled: 10mm diameter x 30mm length Ultraflex Tracheobronchial stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Hospira Inc. Due to Presence...
The Issue: Presence of Particulate Matter: particulate matter identified as an insect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Goldenseal Root 500 mg packaged in a white and orange Recalled by NOW Foods...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Andrographis extract 400 mg packaged in a white and orange Recalled by NOW...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cranberry extract packaged in a white and orange bottle containing Recalled...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Elderberry 500 mg packaged in a white and orange bottle Recalled by NOW...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gingko Biloba 60mg packaged in a white and orange bottle Recalled by NOW...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fenofibrate Capsules (Micronized) 134 mg Recalled by Impax Laboratories,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) 200 mg Recalled by Impax Laboratories,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVIA CHEMISTRY ENZYMATIC CREATININE_2 Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advia Chemistry Assay: Lactate Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Navigation O-arm 02 surgical x-ray imaging system Recalled by...
The Issue: Review of on-system electronic product labeling and Instr uctions for Use in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Assays: Enzymatic Creatine (ECRE) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advia Chemistry Assays - Cholesterol_2 concentrated and Cholesterol Recalled...
The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.