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 1688116900 of 47,632 recalls

Medical DeviceAugust 31, 2020· Encore Medical, LP

Recalled Item: AltiVate Reverse Small Socket Insert Recalled by Encore Medical, LP Due to...

The Issue: Product mislabeled. Use may result in a delay in surgery, stopping of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...

The Issue: The inner lumen of the Langston catheter may separate from the hub during...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 31, 2020· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheter Recalled by Vascular Solutions, Inc. Due to The...

The Issue: The inner lumen of the Langston catheter may separate from the hub during...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 31, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to...

The Issue: The CHF-CB30S Device did not have a 510(k) clearance. Additionally, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...

The Issue: The inner lumen of the Langston catheter may separate from the hub during...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 31, 2020· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...

The Issue: The inner lumen of the Langston catheter may separate from the hub during...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 31, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: DISCOVERY ULTRA Advanced Staining System (RUO-Research Use Only) Material...

The Issue: Potential for Fluid leaks within the instruments, creating an electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Cook Inc.

Recalled Item: Pediatric Nephrostomy Stent Set Recalled by Cook Inc. Due to The indwell...

The Issue: The indwell time for the Percutaneous Neonatal Pigtail Nephrostomy Set and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Cook Inc.

Recalled Item: Percutaneous Neonatal Pigtail Nephrostomy Set Recalled by Cook Inc. Due to...

The Issue: The indwell time for the Percutaneous Neonatal Pigtail Nephrostomy Set and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Brainlab AG

Recalled Item: Ultrasound Navigation Software 1.0 and Ultrasound Integration Software for...

The Issue: Brainlab Ultrasound Navigation Software does not support the modification of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: BenchMark ULTRA Advanced Staining System (IVD)- Material Number: 05342716001...

The Issue: Potential for Fluid leaks within the instruments, creating an electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Ultradent Products, Inc.

Recalled Item: PermaFlo Flowable Composite 948 Shade: A2 - Product Usage: Recalled by...

The Issue: Due to a potential manufacturing issue (cross contamination), composite is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Medical Systems Corporation (OMSC) Evis Exera II Bronchovideoscope...

The Issue: The BF-Q180 bronchoscope is being recalled because it does not have a 510(k)...

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

Class II — Potential Health HazardOngoing
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: 365 Whole Foods Market Organic Reduced fat &Sodium Popcorn Recalled by EAGLE...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: 365 Everyday Value Organic Classic Salted Popcorn Recalled by EAGLE FAMILY...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: Nice! Organic White Cheddar Popcorn Recalled by EAGLE FAMILY FOODS GROUP LLC...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: Cretors Organic Extra Virgin Olive Oil Popcorn Recalled by EAGLE FAMILY...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: 365 Whole Foods Market Organic White Cheddar Popcorn Recalled by EAGLE...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: Nature's Promise Organic Lightly Salted Popcorn Recalled by EAGLE FAMILY...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· Preferred Popcorn

Recalled Item: Organic Yellow Popcorn packaged in the following ways: 1) Great Recalled by...

The Issue: Popcorn may contain foreign material: tempered glass between 3 mm and 7 mm...

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

Class II — Potential Health HazardOngoing
Refund