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. 2,386 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,386 in last 12 months

Showing 2146121480 of 47,632 recalls

FoodMay 3, 2019· Back Roads Food Company

Recalled Item: Back Roads Granola: Ancient Grains Best by date: 01/11/20-02/2/20 In 10 oz...

The Issue: Products may contain pieces of aluminum.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 3, 2019· Back Roads Food Company

Recalled Item: Back Roads Granola: Coconut Ginger Best by date: 01/11/20-02/2/20 In 10 oz...

The Issue: Products may contain pieces of aluminum.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets USP 100 mg 1000 film coated tablets Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2019· Avella of Deer Valley, Inc. Store 38

Recalled Item: Bevacizumab 2.5 mg/0.1 mL Recalled by Avella of Deer Valley, Inc. Store 38...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets USP 100 mg 90 film coated tablets Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Heritage Pharmaceuticals, Inc. Due to...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets USP 50 mg 90 film coated tablets Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets USP 25 mg 90 film coated tablets Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 3, 2019· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...

The Issue: Users with Android OS 8.0 and above may be unable to transfer values...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2019· XTANT MEDICAL INC

Recalled Item: OsteoSelect Demineralized Bone Matrix (DBM) Putty 10.0cc in a syringe...

The Issue: The firm received one customer complaint concerning three OsteoSelect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2019· Monarch Medical Technologies

Recalled Item: Monarch Medical Technologies EndoTool IV Recalled by Monarch Medical...

The Issue: Insulin dosing calculations were erroneously high.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Membrane Changer Insert [5 pcs - Product Usage: is Recalled by SenTec...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Oakworks Inc

Recalled Item: OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401 Recalled by Oakworks Inc Due...

The Issue: Table assembly error with incorrect actuators for the lateral and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Standard Starter Set with and without Service Gas (2 Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

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

Class II — Potential Health HazardOngoing