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. 2,516 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,516 in last 12 months

Showing 92019220 of 13,354 recalls

DrugJanuary 8, 2016· Perrigo Company PLC

Recalled Item: Guaifenesin Grape liquid 100 mg/5 mL Recalled by Perrigo Company PLC Due to...

The Issue: Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2016· Mayne Pharma Usa

Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Mayne Pharma Usa Due to Lack...

The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness test

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2016· Hospira Inc.

Recalled Item: Magnesium Sulfate in Water for Injection Recalled by Hospira Inc. Due to...

The Issue: Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 31, 2015· Sandoz Inc

Recalled Item: Candesartan Cilexetil Tablets Recalled by Sandoz Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; 9 month stability timepoint

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

Class III — Low RiskOngoing
Refund
DrugDecember 31, 2015· Pharmedium Services, LLC

Recalled Item: NORepinephrine Bitartrate Recalled by Pharmedium Services, LLC Due to...

The Issue: Subpotent Drug; confirmed results by FDA analysis after customer complaints...

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

Class III — Low RiskOngoing
Refund
DrugDecember 31, 2015· Pharmedium Services, LLC

Recalled Item: NORepinephrine Bitartrate Recalled by Pharmedium Services, LLC Due to...

The Issue: Subpotent Drug; confirmed results by FDA analysis after customer complaints...

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

Class III — Low RiskOngoing
Refund
DrugDecember 24, 2015· Macleods Pharma Usa Inc

Recalled Item: Pramipexole Dihydrochloride Tablets 0.125 mg Recalled by Macleods Pharma Usa...

The Issue: Presence of Foreign Tablets/Capsules: Presence of a comingled Carbimazole 5...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2015· Nuway Distributors, LLC

Recalled Item: APEXXX tablets Recalled by Nuway Distributors, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2015· Teva North America

Recalled Item: Capecitabine tablets USP 500 mg Recalled by Teva North America Due to Failed...

The Issue: Failed Dissolution Specifications: low test results at the 18 month time-point

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2015· National Vitamin Co Inc

Recalled Item: Life-Line DOCUSATE CALCIUM Sodium Free STOOL SOFTENER 240 mg each Recalled...

The Issue: Labeling: Label mix-up. Docusate Sodium 100mg Softgels were mislabeled as...

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

Class III — Low RiskOngoing
Refund
DrugDecember 17, 2015· Bio-pharm, Inc.

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by Bio-pharm, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications: Product recalled due to...

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

Class III — Low RiskOngoing
Refund