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 2566125680 of 47,632 recalls

DrugFebruary 21, 2018· Akorn, Inc.

Recalled Item: Atropine Sulfate Ophthalmic 1% Solution Recalled by Akorn, Inc. Due to...

The Issue: Failed Stability Specification: OOS low viscosity results discovered during...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 21, 2018· Echopixel, Inc.

Recalled Item: True 3D Viewer Recalled by Echopixel, Inc. Due to With certain software...

The Issue: With certain software versions, import of enhanced ultrasound formatted...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2018· Allen Medical Systems

Recalled Item: F-T3SYSTEM Recalled by Allen Medical Systems Due to The recalling firm has...

The Issue: The recalling firm has become aware that the rail section clamps used to...

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

Class II — Potential Health HazardOngoing
DrugFebruary 20, 2018· Hospira Inc. A Pfizer Company

Recalled Item: Labetalol Hydrochloride Injection Recalled by Hospira Inc. A Pfizer Company...

The Issue: Defective Container: Cracked glass at the rim surface of glass vials,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2018· Cardinal Health 200, LLC

Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...

The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza software Syngo.Plaza is a Picture Archiving and Communication...

The Issue: Software upgrade to correct format of study dates and issues with Legacy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2018· Cardinal Health 200, LLC

Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...

The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2018· Cardinal Health 200, LLC

Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...

The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2018· Cardinal Health 200, LLC

Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...

The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza software VB10A model numbers: 10863171 Recalled by Siemens...

The Issue: Software upgrade to correct format of study dates and issues with Legacy...

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

Class II — Potential Health HazardOngoing
FoodFebruary 20, 2018· Lotte International America Corp.

Recalled Item: Lotte Kancho Choco-Biscuit Recalled by Lotte International America Corp. Due...

The Issue: Firm was notified by customer of peanut allergen found in the product during...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 19, 2018· Zimmer Biomet, Inc.

Recalled Item: EBI Osteogen Implantable Bone Growth Stimulator The OsteoGen Implantable...

The Issue: Lack of adequate validation and controls to ensure that product cleanliness...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 19, 2018· Zimmer Biomet, Inc.

Recalled Item: SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini...

The Issue: Lack of adequate validation and controls to ensure that product cleanliness...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 16, 2018· Aesculap Implant Systems LLC

Recalled Item: Strauss Penis Clamp 130MM/General Instruments Recalled by Aesculap Implant...

The Issue: The plastic sleeves of the Penis Clamp and Mouth Gag may stick together...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 16, 2018· Aesculap Implant Systems LLC

Recalled Item: Doyen-Collin Mouth Gag 120MM/ General Instruments Recalled by Aesculap...

The Issue: The plastic sleeves of the Penis Clamp and Mouth Gag may stick together...

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

Class III — Low RiskOngoing
DrugFebruary 16, 2018· B. Braun Medical Inc

Recalled Item: 0.9% Sodium Chloride Irrigation USP Recalled by B. Braun Medical Inc Due to...

The Issue: Presence of Particulate Matter: Customer complaint of particulate matter...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2018· Medline Industries Inc

Recalled Item: PVP Scrub Solution Recalled by Medline Industries Inc Due to Subpotent Drug:...

The Issue: Subpotent Drug: product not meeting the iodine assay level requirements...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2018· Seggiano Usa Inc.

Recalled Item: Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g Recalled by...

The Issue: The Tuscan Kale Pesto was mislabeled as Seggiano Artichoke & Garlic Sauce &...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2018· Transonic Systems Inc

Recalled Item: Transonic ADT1018 Flow QC Clear Advantage Tubing Recalled by Transonic...

The Issue: The sterility of the device cannot be assured. There is a potential for an...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due...

The Issue: Following a period of inactivity, the mass storage device may cause the...

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

Class II — Potential Health HazardOngoing