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. 2,349 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,349 in last 12 months

Showing 2970129720 of 47,632 recalls

DrugFebruary 3, 2017· Apotex Inc.

Recalled Item: CycloSPORINE Capsules Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Impurities/Degradations Specifications; out of specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 3, 2017· Amerisource Health Services

Recalled Item: GlipiZIDE Extended-release tablets Recalled by Amerisource Health Services...

The Issue: Failed dissolution specifications: Glipizide 2.5 mg ER Tablets exceeded...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 750 mg added to 5% Dextrose 250 mL For IV Use Only Recalled...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1.25 g added to 0.9% Sodium Chloride 250 mL Bag For IV Use...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1 g added to 0.9% Sodium Chloride 250 mL Bag For IV Use Only...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1.5 gram added to 5% Dextrose 500 mL Recalled by SCA...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1.25 g added to 5% Dextrose 250 mL Bag For IV Use Only...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 750 mg added to 250 mL 0.9% Sodium Chloride For IV Use Only...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 2, 2017· Sage Products Inc

Recalled Item: Q Care Continue Care Kit for the non-ventilated patient Recalled by Sage...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The expiration date of...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2017· Sandoz Inc

Recalled Item: Transderm Scop (scopolamine) Transdermal System Recalled by Sandoz Inc Due...

The Issue: Labeling: Incorrect Instructions:outer carton contains the incorrect...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 2, 2017· Teva Pharmaceuticals USA

Recalled Item: Mimvey Lo (estradiol and norethindrone acetate tablets USP) Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: out of specification test...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 2, 2017· Elcam Medical, Inc.

Recalled Item: Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w...

The Issue: The stopcock was found to have punctures.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Check-Flo Hemostasis Assembly Recalled by Cook Inc. Due to Devices using a...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Micropuncture Check-Flo Performer Introducer Set Recalled by Cook Inc. Due...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing