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. 2,259 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,259 in last 12 months

Showing 4578145800 of 47,632 recalls

FoodSeptember 18, 2012· Dale & Thomas Popcorn, LLC

Recalled Item: Popcorn Indiana Bacon Ranch Popcorn Net Wt. 3.5 oz - Recalled by Dale &...

The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2012· Dale & Thomas Popcorn, LLC

Recalled Item: Popcorn Indiana Almond Biscotti Caramel Popcorn Net Wt. 6.5 oz. Recalled by...

The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2012· Dale & Thomas Popcorn, LLC

Recalled Item: Popcorn Indiana American Cheese Popcorn Net Wt. 7 oz. Recalled by Dale &...

The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2012· Dale & Thomas Popcorn, LLC

Recalled Item: Popcorn Indiana Wasabi Reserve Popcorn Net Wt. 5.5 oz Recalled by Dale &...

The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2012· Dale & Thomas Popcorn, LLC

Recalled Item: Popcorn Indiana Drizzled Black & White Kettlecorn Net Wt. 6 Recalled by Dale...

The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2012· Dale & Thomas Popcorn, LLC

Recalled Item: Popcorn Indiana Salt and Pepper Popcorn Net Wt. 6.9 oz Recalled by Dale &...

The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2012· Dale & Thomas Popcorn, LLC

Recalled Item: Popcorn Indiana Apple Crisp Popcorn Net Wt. 6.5 oz. Recalled by Dale &...

The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2012· Dale & Thomas Popcorn, LLC

Recalled Item: Popcorn Indiana Chocolate Peanut Butter Kettlecorn Net Wt 5 oz. Recalled by...

The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2012· Dale & Thomas Popcorn, LLC

Recalled Item: Popcorn Indiana Drizzled Cinnamon Sugar Kettlecorn Net Wt. 5.5 oz. Recalled...

The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 18, 2012· Iris Diagnostics

Recalled Item: Iris Diagnostics Division iQ Control/Focus Set Recalled by Iris Diagnostics...

The Issue: The firm initiated this recall because complaints from customers reported...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental Kodak 2200 Intraoral X-ray system Product Usage: The...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental CS 2100 X-ray system Product Usage: The expected Recalled...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental Kodak 2100 Intraoral X-ray system Product Usage: The...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental CS 2200 X-ray system Product Usage: The expected Recalled...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Instratek, Incorporated

Recalled Item: Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The...

The Issue: Instratek, Inc.has received multiple complaints of the 1052 Trigger Finger...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by...

The Issue: The low contrast pins in the Image Quality (IQ) phantom deteriorates over...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Elekta, Inc.

Recalled Item: MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR)...

The Issue: A patient was seriously mistreated after a user made and saved an...

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

Class II — Potential Health HazardOngoing
DrugSeptember 17, 2012· DermaCare, Inc.

Recalled Item: UP & UP brand Recalled by DermaCare, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non-Sterile Products: Laboratory findings of high...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2012· DermaCare, Inc.

Recalled Item: UP & UP brand Recalled by DermaCare, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non-Sterile Products: Laboratory findings of high...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab¿ 1265 system blood gas analyzer Product Usage: RAPIDLab...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing