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. 1,670 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,670 in last 12 months

Showing 4220142220 of 47,632 recalls

Medical DeviceSeptember 30, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic Activa PC Recalled by Medtronic Neuromodulation Due to Medtronic...

The Issue: Medtronic notified customers regarding over stimulation or stimulation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Rim Impactor Tip Product Usage: Used for MDM Recalled...

The Issue: Stryker has received complaints associated with cracks and/or fracture of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Draeger Medical, Inc.

Recalled Item: Draeger Movita 603x/DVE 803x Ceiling Supply Unit. It is intended Recalled by...

The Issue: Cases were encountered with the Draeger Movita 603x/DVE 803x Ceiling Supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic Activa PC Recalled by Medtronic Neuromodulation Due to Medtronic...

The Issue: Medtronic notified customers regarding Loss of Stimulation of specific...

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

Class II — Potential Health HazardOngoing
DrugSeptember 30, 2013· G & W Laboratories Inc

Recalled Item: G & W Fluocinolone Acetonide Cream USP 0.025% Recalled by G & W Laboratories...

The Issue: Failed Content Uniformity Specifications; at the 18 month time point.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2013· Haute Health, LLC

Recalled Item: Prolifta Dietary Supplement Prolifta Recalled by Haute Health, LLC Due to...

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 27, 2013· Haute Health, LLC

Recalled Item: Virilis Pro Recalled by Haute Health, LLC Due to Marketed without an...

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 27, 2013· Haute Health, LLC

Recalled Item: PHUK Sexual Enhancement Ultimate Pleasure Recalled by Haute Health, LLC Due...

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may contain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 27, 2013· Insulet Corporation

Recalled Item: OmniPod Insulin Management Product Demonstration Kit Recalled by Insulet...

The Issue: Alcohol Prep Pads contained within the kit are not properly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2013· Insulet Corporation

Recalled Item: OmniPod Insulin Management System Starter Kit Recalled by Insulet...

The Issue: Alcohol Prep Pads contained within the kit are not properly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2013· Cordis Corporation

Recalled Item: Cordis OPTEASE Vena Cava Filter Is indicated for use in Recalled by Cordis...

The Issue: Cordis identified a printing error on one unit of the Optease Vena Cava...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2013· B. Braun Medical, Inc.

Recalled Item: B. Braun Introcan Safety IV Catheter PUR 24G Recalled by B. Braun Medical,...

The Issue: One lot of Introcan Safety IV Catheters may not contain the anti-needlestick...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2013· Olympus America Inc.

Recalled Item: TB-0545PC: THUNDERBEAT 5 mm Recalled by Olympus America Inc. Due to...

The Issue: Complaints of damage to various models of Thunderbeat Hand Instruments...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2013· S.A.E. AFIKIM

Recalled Item: Breeze C Scooter is a motorized electric scooter for elderly Recalled by...

The Issue: Breeze C Scooter, motorized 3-wheeled electric scooter for elderly people,...

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

Class II — Potential Health HazardOngoing
FoodSeptember 27, 2013· Big Blue Fisheries

Recalled Item: Hickory Smoked Coho Salmon is sold in vacuum packed plastic packages...

The Issue: Big Blue Fisheries, LLC. is recalling ALL smoked products from all lots and...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 27, 2013· Big Blue Fisheries

Recalled Item: Smoked King Salmon Bellies is sold in vacuum packed plastic packages...

The Issue: Big Blue Fisheries, LLC. is recalling ALL smoked products from all lots and...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 27, 2013· Big Blue Fisheries

Recalled Item: Pepper Smoked King Salmon. Product sold in vacuum packed plastic packages...

The Issue: Big Blue Fisheries, LLC. is recalling ALL smoked products from all lots and...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 27, 2013· Big Blue Fisheries

Recalled Item: Smoked Coho Salmon Bellies is sold in vacuum packed plastic packages...

The Issue: Big Blue Fisheries, LLC. is recalling ALL smoked products from all lots and...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 27, 2013· Big Blue Fisheries

Recalled Item: Variety Smoked Pack is sold in vacuum packed plastic packages Recalled by...

The Issue: Big Blue Fisheries, LLC. is recalling ALL smoked products from all lots and...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 27, 2013· Big Blue Fisheries

Recalled Item: Teriyaki Smoked Coho Salmon is sold in vacuum packed plastic packages...

The Issue: Big Blue Fisheries, LLC. is recalling ALL smoked products from all lots and...

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

Class II — Potential Health HazardOngoing
Refund