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. 2,360 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,360 in last 12 months

Showing 2520125220 of 47,632 recalls

FoodApril 18, 2018· Viable Solutions, LLC

Recalled Item: Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa...

The Issue: Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 18, 2018· Viable Solutions, LLC

Recalled Item: Mitragyna Speciosa Leaf Powder-GREEN Horn Recalled by Viable Solutions, LLC...

The Issue: Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 17, 2018· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators Recalled by...

The Issue: There is a potential for the cord to spark and cause a fire.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 17, 2018· Rhodes Pharmaceuticals, L.P.

Recalled Item: Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only...

The Issue: Failed Dissolution Specification: Low dissolution outside of specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 16, 2018· Epic Products, LLC

Recalled Item: Euphoric Premium Male Performance Enhancer capsules Recalled by Epic...

The Issue: Marketed Without An Approved NDA/ANDA: product contains undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodApril 16, 2018· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Multiple products marketed...

The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 16, 2018· Grand Canyon Foods International LLC.

Recalled Item: Southwestern Gourmet Butter Popcorn Grand Canyon Foods Recalled by Grand...

The Issue: An FDA inspection revealed products that contained Yellow 5 and soy lecithin...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 16, 2018· Grato Holdings, Inc.

Recalled Item: Peaceful Mountain Recalled by Grato Holdings, Inc. Due to Multiple products...

The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 16, 2018· Grato Holdings, Inc.

Recalled Item: Peaceful Mountain -Stomach Rescue - Dietary supplement - Elemental silver...

The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 16, 2018· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Multiple products marketed...

The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 16, 2018· Grand Canyon Foods International LLC.

Recalled Item: Southwestern Gourmet Prickly Pear Popcorn Grand Canyon Foods Recalled by...

The Issue: An FDA inspection revealed products that contained Yellow 5 and soy lecithin...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Promote Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· Cook Inc.

Recalled Item: Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter Recalled by Cook...

The Issue: Incorrect product labeling. Product labeled as 6mm x 2cm balloon are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· Bard Peripheral Vascular Inc

Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...

The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· Bard Peripheral Vascular Inc

Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...

The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor Recalled by St Jude...

The Issue: The firm is advising physicians that exposure to sub-freezing temperatures...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Merlin PCS Programmer Software: 3330 The Merlin PCS programmer (model...

The Issue: The firm is advising physicians that exposure to sub-freezing temperatures...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Merlin PCS programmer (Model # 3650) Recalled by St Jude Medical Inc. Due to...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Unify Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Fortify Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing