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. 2,442 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,442 in last 12 months

Showing 1698117000 of 47,632 recalls

Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: First Check 4 Panel Drug Cup: COC/MET1000/OPI2000/THC): (THC/COC) Recalled...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Alere iScreen Single Drug Detection (AMT Item Number/ AMT Description):...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Alere iScreen Multi Drug Detection (AMT Item Number/ AMT Description):...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: MicroTox (AMT Item Number/ AMT Description): MTPA-6MBAU / "MicroTox...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Oratect III Oral Fluid Drug Screen Device (AMT Item Number/ Recalled by...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: MicroScreen (AMT Item Number/ AMT Description): MSCA-6MBAU/ "MicroScreen...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Alere iCup Drug Detection (AMT Item Number/ AMT Description): I-DXA-10/...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Fastect¿ II Drug Screen Dipstick Test Single Drug Detection (AMT Recalled by...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: First Check 1 Panel Drug Cup: (THC) Recalled by Ameditech Inc Due to Various...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: CLIA Waived Rapid Drug Test (AMT Item Number/ AMT Description): Recalled by...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

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

Class II — Potential Health HazardOngoing
DrugAugust 17, 2020· Maison Terre, LLC

Recalled Item: Goldenseal Root Powder Organic Recalled by Maison Terre, LLC Due to...

The Issue: Microbial Contamination of Non-Sterile Products: FDA laboratory analysis...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 17, 2020· Mylan Institutional LLC

Recalled Item: Tranexamic Acid Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 17, 2020· Mylan Institutional LLC

Recalled Item: Amiodarone Hydrochloride Injection Recalled by Mylan Institutional LLC Due...

The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2020· Grupo Asimex de Mexico SA de CV

Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...

The Issue: Chemical Contamination: FDA analysis found the product contains methanol,...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2020· Grupo Asimex de Mexico SA de CV

Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...

The Issue: CGMP Deviations: All other lots are being recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 14, 2020· SG24 LLC

Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottle with foam pump Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2020· SG24 LLC

Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand Sanitizing Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2020· SG24 LLC

Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 10 mL Pocket Pen Dist by: SG24 LLC...

The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2020· SG24 LLC

Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump Recalled...

The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: Buprenorphine HCl Injection Recalled by Hikma Pharmaceuticals USA Inc. Due...

The Issue: Sub-potent Drug: Out-of-Specification assay results found at 3 month...

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

Class II — Potential Health HazardOngoing
Refund