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. 2,260 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,260 in last 12 months

Showing 4520145220 of 47,632 recalls

FoodDecember 7, 2012· Sugar Flowers Plus

Recalled Item: Pastillage (gum paste) Flowers Recalled by Sugar Flowers Plus Due to...

The Issue: Sugar Flowers Plus Inc of Glendale, CA is recalling Cake Decors Pastillage...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2012· Sugar Flowers Plus

Recalled Item: Pastillage (gum paste) Flowers Recalled by Sugar Flowers Plus Due to...

The Issue: Sugar Flowers Plus Inc of Glendale, CA is recalling Cake Decors Pastillage...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2012· Sugar Flowers Plus

Recalled Item: Pastillage (gum paste) Flowers Recalled by Sugar Flowers Plus Due to...

The Issue: Sugar Flowers Plus Inc of Glendale, CA is recalling Cake Decors Pastillage...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2012· Sugar Flowers Plus

Recalled Item: Pastillage (gum paste) Flowers Recalled by Sugar Flowers Plus Due to...

The Issue: Sugar Flowers Plus Inc of Glendale, CA is recalling Cake Decors Pastillage...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 6, 2012· Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Recalled Item: Hydrocodone bitartrate and acetaminophen Tablets Recalled by Vintage...

The Issue: Superpotent (Multiple Ingredient) Drug: Complaint received of oversized tablets.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 6, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Emit(R) tox(TM) Serum Calibrators Recalled by Siemens Healthcare...

The Issue: Incorrect expiration date was assigned to the D1 lot of Emit(R) tox(TM)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 6, 2012· Hill-Rom, Inc.

Recalled Item: Liko Standard Slingbar 450. The Standard Slingbar 450 is a Recalled by...

The Issue: Liko/Hill-Rom has received reports from facilities which indicate that...

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

Class II — Potential Health HazardOngoing
DrugDecember 5, 2012· Teva Pharmaceuticals USA, Inc.

Recalled Item: Copaxone (glatiramer acetate injection) Recalled by Teva Pharmaceuticals...

The Issue: Presence of Foreign Substance: Product is being recalled due to receiving an...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 5, 2012· West-ward Pharmaceutical Corp.

Recalled Item: PredniSONE Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: Tablets are being recalled due to gray...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 5, 2012· West-ward Pharmaceutical Corp.

Recalled Item: PredniSONE Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: A complaint was received for black specks...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 5, 2012· B Braun Medical, Inc.

Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...

The Issue: B. Braun Medical Inc. is informing our customers of a field correction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2012· Canon Inc.

Recalled Item: Canon Full Auto RK-F2 Recalled by Canon Inc. Due to Canon Inc. had received...

The Issue: Canon Inc. had received 17 claims from our foreign sales companies between...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2012· SynCardia Systems Inc.

Recalled Item: Companion External Battery Recalled by SynCardia Systems Inc. Due to...

The Issue: Syncardia Systems is recalling the Companion External Batteries used with...

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

Class II — Potential Health HazardOngoing
DrugDecember 4, 2012· Green Valley Drugs

Recalled Item: Cyanocobalamin 1000 mcg/ml Recalled by Green Valley Drugs Due to...

The Issue: Non-Sterility: Green Valley Drugs received positive sterility results from...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2012· Green Valley Drugs

Recalled Item: Methylprednisolone Preservative Free 40 mg/ml Injectible Suspension Recalled...

The Issue: Non-Sterility: Green Valley Drugs received positive sterility results from...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Abbott Laboratories

Recalled Item: Synthroid (Levothyroxine Sodium) tablets Recalled by Abbott Laboratories Due...

The Issue: Labeling: Error on Declared Strength. Product labeled to contain 150 mcg...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Johnson & Johnson

Recalled Item: Clean & Clear advantage Recalled by Johnson & Johnson Due to Superpotent...

The Issue: Superpotent (Single Ingredient Drug): salicylic acid

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

Class III — Low RiskOngoing
Refund