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. 2,512 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,512 in last 12 months

Showing 99219940 of 47,632 recalls

DrugDecember 27, 2022· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Prochlorperazine Maleate Tablets Recalled by Jubilant Cadista...

The Issue: Subpotent Drug: Out of specification for assay at the 18-month stability...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 27, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Medline Sterile Hand Pack Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The convenience trays had improper placement of some of the components that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Sterile Oncology Port Access Tray Recalled by MEDLINE INDUSTRIES, LP...

The Issue: The convenience trays had improper placement of some of the components that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Medline Sterile Maximum Barrier Pack-LF Recalled by MEDLINE INDUSTRIES,...

The Issue: The convenience trays had improper placement of some of the components that...

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

Class II — Potential Health HazardOngoing
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Adventure Marine 150 Recalled by GFA Production Xiamen Co. Ltd. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid Class A ANSI 25 Person Recalled by GFA Production Xiamen...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Adventure First Aid 1.5 Recalled by GFA Production Xiamen Co. Ltd. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid 25 Person 2009 ANSI Recalled by GFA Production Xiamen...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid 10 Person 2009 ANSI Recalled by GFA Production Xiamen...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: CVS First Aid Home Recalled by GFA Production Xiamen Co. Ltd. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid 25 Person 2009 ANSI Recalled by GFA Production Xiamen...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid 10 Person 2009 ANSI Recalled by GFA Production Xiamen...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Adventure First Aid 1.0 Recalled by GFA Production Xiamen Co. Ltd. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care first aid Burn Cream (benzalkonium chloride 0.13% and Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 23, 2022· Philips Healthcare (Suzhou) Co., Ltd.

Recalled Item: Incisive CT Recalled by Philips Healthcare (Suzhou) Co., Ltd. Due to...

The Issue: Multiple software issues which have the potential to lead to misdiagnosis...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2022· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LinkSymphoKnee Distal Femoral Augment - Tilastan - Size. 7-8 Recalled by...

The Issue: Fixation screw was inserted through the wrong side of the augment (distal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2022· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LinkSymphoKnee Distal Femoral Augment - Tilastan - Size 7-8 Recalled by...

The Issue: Fixation screw was inserted through the wrong side of the augment (distal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2022· Quest Medical, Inc.

Recalled Item: Precision Delivery Set with Filter Recalled by Quest Medical, Inc. Due to...

The Issue: Delivery Sets may have tubing that could become detached that could result...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTURION MEDICAL PRODUCTS Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: The kit contained an expired component.

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

Class II — Potential Health HazardOngoing
DrugDecember 22, 2022· Pharmacy Innovations

Recalled Item: Minoxidil 0.75% (1.5ML vial) Injectable Recalled by Pharmacy Innovations Due...

The Issue: Lack of Assurance of Sterility: FDA inspection revealed insanitary...

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

Class II — Potential Health HazardOngoing
Refund