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. 2,534 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,534 in last 12 months

Showing 45014520 of 13,354 recalls

DrugJune 16, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: Childrens Dimetapp Cold & Cough Recalled by Glaxosmithkline Consumer...

The Issue: Defective Delivery System: the dosing cups are missing graduations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 13, 2020· Yusef Manufacturing Laboratories, LLC

Recalled Item: Tropical Lip Moisturizer Recalled by Yusef Manufacturing Laboratories, LLC...

The Issue: Superpotent Drug: The beginning portion of the batch appears to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· Beaming White Llc

Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl

The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· The Harvard Drug Group

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by The Harvard...

The Issue: CGMP Deviation: Potential presence of Nitrosodimethylamine (NDMA) Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· Beaming White Llc

Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl

The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· Beaming White Llc

Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl

The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Clozapine Tablets USP tablet Recalled by Aurobindo Pharma USA Inc. Due to...

The Issue: Presence of foreign tablet: Consumer complaint of Clozapine Tablets 50mg...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Defective Container: Customer complaints received of a crimp defect while...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Defective Container: Customer complaints received of a crimp defect while...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2020· American Health Packaging

Recalled Item: Nabumetone Tablets Recalled by American Health Packaging Due to Labeling Not...

The Issue: Labeling Not Elsewhere Classified: The statement Pharmacist: Dispense with...

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

Class III — Low RiskOngoing
Refund
DrugJune 10, 2020· Alembic Pharmaceuticals Limited

Recalled Item: Aripiprazole Tablets Recalled by Alembic Pharmaceuticals Limited Due to...

The Issue: Labeling: Label mix up: Bottles labeled as aripiprazole 2 mg, 30 count had...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2020· Crown Laboratories

Recalled Item: Nystatin Cream Recalled by Crown Laboratories Due to Subpotent Drug: Out of...

The Issue: Subpotent Drug: Out of specification for assay at the 9-month interval for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2020· Crown Laboratories

Recalled Item: Nystatin Cream Recalled by Crown Laboratories Due to Subpotent Drug: Out of...

The Issue: Subpotent Drug: Out of specification for assay at the 9-month interval for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2020· Akorn, Inc.

Recalled Item: Prednisolone Sodium Phosphate Oral Solution Recalled by Akorn, Inc. Due to...

The Issue: Discoloration: Out of Specification (OOS) result for APHA Color Test.

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

Class III — Low RiskOngoing
Refund
DrugJune 5, 2020· Marksans Pharma Limited

Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 4, 2020· AVKARE Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by AVKARE Inc. Due...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 4, 2020· SOMERSET THERAPEUTICS LLC

Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...

The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...

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

Class III — Low RiskOngoing
Refund
DrugJune 4, 2020· SOMERSET THERAPEUTICS LLC

Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...

The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...

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

Class III — Low RiskOngoing
Refund
DrugJune 4, 2020· AVKARE Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by AVKARE Inc. Due...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 4, 2020· SOMERSET THERAPEUTICS LLC

Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...

The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...

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

Class III — Low RiskOngoing
Refund