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 2092120940 of 47,632 recalls

DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: TUSSLIN (Dextromethorphan HBr Recalled by Pharma-Natural Inc. Due to CGMP...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: ARMY HEALTH With CURCUMIN (Menthol 3.00%) Pain Reliever Roll-On Recalled by...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: Oliver's Harvest CBD+Capsaicin 0.2% Pain Relief (Capsaicin 0.2%) Topical...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: DOUBLE TUSSIN DM (Dextromethorphan Hbr 20 mg Recalled by Pharma-Natural Inc....

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: Oliver's Harvest CBD+Lidocaine HCL 4% Pain Relief (Lidocaine HCL 4%)...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: SORBUGEN NR (Dextromethorphan HBr Recalled by Pharma-Natural Inc. Due to...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: Lid O Creme (Lidocaine HCL 4% and Menthol 1%) Topical Analgesic Cream...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: Dermanak original crema blanqueador (Hydroquinone 2%) Skin Fade Cream...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: Workvie Instant Pain Relieving Roll On (Lidocaine HCL 4% + Menthol 1% &...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: AbeeMed cream (Menthol 1.48% and Histamine DHCL 0.05%) Recalled by...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: Lido E.R. (Lidocaine HCL 4%) Pain Relieving Topical Analgesic Cream Recalled...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 21, 2019· Pharma-Natural Inc.

Recalled Item: Dayma SUPER FORTE XL10 (Camphor 0.5% Recalled by Pharma-Natural Inc. Due to...

The Issue: CGMP Deviations: products were manufactured with lack of process validation,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 21, 2019· Alto Development Corp

Recalled Item: A&E Medical Corp. Ultra-Flex MYO/Wire Ultra-Flex Monopolar Pacing Wire...

The Issue: Updated instructions for use: Ultra-Flex MYO/WIRE Monopolar pacing wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
FoodJune 20, 2019· Perrigo Company PLC

Recalled Item: Parent's Choice Advantage Infant Formula Milk-Based Powder with Iron...

The Issue: Product may contain metal fragments.

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

Class II — Potential Health HazardOngoing
Refund