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. 2,266 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,266 in last 12 months

Showing 4292142940 of 47,632 recalls

DrugJuly 22, 2013· Torrent Pharma Inc

Recalled Item: Olanzapine Tablets Recalled by Torrent Pharma Inc Due to Defective...

The Issue: Defective Container; This action is being taken as a precautionary measure...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 22, 2013· New Sun Inc

Recalled Item: New Sun Immune 101 Recalled by New Sun Inc Due to Potential E. coli...

The Issue: Positive E.coli

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 22, 2013· New Sun Inc

Recalled Item: New Sun JLB Combination Recalled by New Sun Inc Due to Potential E. coli...

The Issue: Positive E.coli

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Tapered Navigator Certain Surgical Kit Product Usage: Molded plastic tray...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Navigator Surgical Kit Product Usage: Molded plastic tray used in Recalled...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit Product Usage: Molded plastic tray used...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit For Certain Internal Connection Product...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit For Certain and External Connection Product...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Synthes USA HQ, Inc.

Recalled Item: 3.7mm and 5.0mm Dynamic Locking Screw (DLS) Product Usage: 3.7mm Recalled by...

The Issue: All lots of 3.7mm and 5.0mm Dynamic Locking Screw (DLS) were recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· MCKESSON TECHNOLOGIES INC

Recalled Item: Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense...

The Issue: The firm issued a clinical alert after users reported an issue where the...

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

Class II — Potential Health HazardOngoing
FoodJuly 20, 2013· SensoryEffects Powder Systems

Recalled Item: Maple flavored lipid-based inclusions. Maple NT-RF and Maple NT-MF Recalled...

The Issue: The firm was notified by a customer that a random sample from lot 2013-36707...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Siloutte Suplemento Alimenticio Recalled by Herbal Give Care Llc...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelin Siloutte Mezcal Herbal con L-Carnitine Suplemento Alimenticio...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelin Siloutte Te Recalled by Herbal Give Care Llc Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Fem Mezcla con L-Carnitina Suplemento Alimenticio Recalled by...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Man Herbal Blend With L-Carnitine Dietary Supplement Recalled by...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Myson Corporation, Inc.

Recalled Item: Volcano Male Enhancement 1500mg Recalled by Myson Corporation, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: All lots of Volcano Liquid and...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Myson Corporation, Inc.

Recalled Item: Volcano Male Enhancement Liquid Recalled by Myson Corporation, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: All lots of Volcano Liquid and...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Bracco Diagnostics Inc

Recalled Item: Tagitol V Barium Sulfate Suspension (40% w/v Recalled by Bracco Diagnostics...

The Issue: Failed Stability Specifications: Tagitol V Barium Sulfate Lot #65846 sampled...

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

Class III — Low RiskOngoing
Refund
DrugJuly 19, 2013· Watson Laboratories Inc

Recalled Item: Oxycodone and Acetaminophen Capsules Recalled by Watson Laboratories Inc Due...

The Issue: Subpotent drug: Two lots of Oxycodone and Acetaminophen Capsules, USP 5/500...

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

Class III — Low RiskOngoing
Refund