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 2640126420 of 47,632 recalls

Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: NovaKone Toric Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP49 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...

The Issue: Contact lenses lack sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Safety Sideport Knife: (a) 1.0mm Recalled by Beaver-Visitec...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Xstar Safety Crescent Recalled by Beaver-Visitec International...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Optimum Safety Sideport Knife: (a) Straight 15o Recalled by...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Xstar Safety Slit Knife: (a) Recalled by Beaver-Visitec...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Medtronic Inc.

Recalled Item: Everflex Self-Expanding Peripheral Stent with Entrust Delivery System...

The Issue: Stent length on the label may not match the length of the stent itself.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Volcano Corporation

Recalled Item: Volcano Imaging System s5i Recalled by Volcano Corporation Due to On certain...

The Issue: On certain Impacted Systems, an unexpected Microsoft Windows Security dialog...

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

Class II — Potential Health HazardOngoing
DrugNovember 3, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: bupPROPion HCL Extended-Release Tablets Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Mylan Pharmaceuticals Inc. is...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 3, 2017· Handicare Usa Inc

Recalled Item: Handicare C Series Patient Lift Product Usage: A device used Recalled by...

The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Handicare Usa Inc

Recalled Item: Handicare P600 Series Patient Lift Product Usage: A device used Recalled by...

The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2017· Pro-Med Instruments Gmbh

Recalled Item: pmi Recalled by Pro-Med Instruments Gmbh Due to The firm received reports of...

The Issue: The firm received reports of two breakages of the pin tips which occurred...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2017· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to The internal...

The Issue: The internal configuration of the electrometers and the Real-Time control...

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

Class II — Potential Health HazardOngoing
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Coffee beans packaged in Bulk 4 oz. Plastic Recalled by...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· doTERRA International, LLC

Recalled Item: Slim & Sassy¿ TrimShake Chocolate Recalled by doTERRA International, LLC Due...

The Issue: doTERRA is voluntarily recalling unexpired Slim & Sassy¿ TrimShake -...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Cranberries packaged in: Bulk 3.5 oz. Plastic Cup Recalled by...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Aurora Brand Dark Chocolate Cherries packaged in: 8.5 oz. Plastic Recalled...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· doTERRA International, LLC

Recalled Item: Slim & Sassy¿ TrimShake Vanilla Recalled by doTERRA International, LLC Due...

The Issue: doTERRA is voluntarily recalling unexpired Slim & Sassy¿ TrimShake -...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Turbinado Almonds w/ Sea Salt packaged in : Recalled by...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Almonds packaged in: 4 oz. Plastic Pouch Recalled by Aurora...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund