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. 1,660 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,660 in last 12 months

Showing 4574145760 of 47,632 recalls

FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Endurance Daily Vanilla Dietary Supplement Packaged under the label:...

The Issue: Protein supplement fails to declare allergen milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Hunger and Weight Vanilla Dietary Supplement Packaged under the labels...

The Issue: Protein supplement fails to declare allergen: milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Rejuvenate Vanilla Dietary Supplement Packaged under the labels Stronger...

The Issue: Protein supplement fails to declare allergen: milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Pure Whey Natural Dietary Supplement Packaged under the labels: Maine...

The Issue: Protein supplement fails to declare allergen milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Fortified Vanilla Dietary Supplement Packaged under the labels Stronger...

The Issue: Protein supplement fails to declare allergen: milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Recovery Natural (also labeled Post Workout) Recalled by Maine Natural...

The Issue: Protein supplement fails to declare allergens: milk, shellfish

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Endurance In Race Lime Dietary Supplement Packaged under the label Recalled...

The Issue: Protein supplement fails to declare allergens: milk and coconut

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Daily Balance Natural Dietary Supplement Packaged under the labels Stronger...

The Issue: Protein supplement fails to declare allergens: milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Pure Whey Chocolate Recalled by Maine Natural Health, Inc. Due to Protein...

The Issue: Protein supplement fails to declare allergen milk

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 21, 2012· Maine Natural Health, Inc.

Recalled Item: Pure Whey Vanilla Recalled by Maine Natural Health, Inc. Due to Protein...

The Issue: Protein supplement fails to declare allergen: milk

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 20, 2012· Genentech Inc

Recalled Item: Nutropin AQ NuSpin 20 (somatropin (rDNA origin) injection} 20 mg/ 2mL...

The Issue: Miscalibrated and/or Defective Delivery System: Genentech has received...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2012· Globe All Wellness, LLC

Recalled Item: SLIM XTREME Herbal Slimming Capsule Recalled by Globe All Wellness, LLC Due...

The Issue: Marketed Without an Approved NDA/ANDA: Product tested positive for...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 20, 2012· Genentech Inc

Recalled Item: Nutropin AQ NuSpin 10 (somatropin (rDNA origin) injection} 10 mg/ 2mL...

The Issue: Miscalibrated and/or Defective Delivery System: Genentech has received...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2012· Sandoz Incorporated

Recalled Item: Children's Cetirizine HCl Chewable Tablets 5 mg Recalled by Sandoz...

The Issue: Impurity/Degradation; exceeded impurity specification at the 8 and 15 month...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware that patient mismatch without a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Brivo XR 285 Mobile general purpose radiographic imaging...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Sorin Group USA, Inc.

Recalled Item: SCP Pump Control Panel Recalled by Sorin Group USA, Inc. Due to Sorin Group...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 220amx Mobile general purpose radiographic imaging...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Zimmer, Inc.

Recalled Item: The Trilogy Acetabular System Shell with Cluster Holes Porous 56 Recalled by...

The Issue: Zimmer Trilogy¿ Acetabular System Shell with Cluster Holes, Porous,56 MM...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 200amx with digital upgrade Mobile general Recalled...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing