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 4518145200 of 47,632 recalls

Medical DeviceDecember 13, 2012· Ortho-Clinical Diagnostics

Recalled Item: Ortho Clinical Diagnostics VITROS¿ Chemistry Products Vapor Adsorption...

The Issue: Some VITROS¿ Chemistry Products Vapor Adsorption Cartridge CAT No. 6800100...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2012· Philips Healthcare Inc.

Recalled Item: Juno DRF Recalled by Philips Healthcare Inc. Due to Values of fluoroscopy...

The Issue: Values of fluoroscopy time, Air Kerma Rate and Cumulated Air Kerma may not...

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

Class II — Potential Health HazardOngoing
DrugDecember 12, 2012· Schering-Plough Products, LLC

Recalled Item: Temodar (temozolomide) Capsule Recalled by Schering-Plough Products, LLC Due...

The Issue: Failed Impurities/Degradation Specifications: The recall is being initiated...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2012· Boehringer Ingelheim Roxane Inc

Recalled Item: Perindopril Erbumine Tablets Recalled by Boehringer Ingelheim Roxane Inc Due...

The Issue: Impurities/Degradation Products: Out of Specification results found for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 12, 2012· Abbott Laboratories

Recalled Item: Abbott Laboratories Recalled by Abbott Laboratories Due to The Architect...

The Issue: The Architect 25-OH Vitamin D assay has the potential to generate falsely...

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

Class II — Potential Health HazardOngoing
FoodDecember 11, 2012· Whole Foods Market

Recalled Item: Natures Path Hemp Plus Granola sold in bulk bins at Whole Foods PLU 8106...

The Issue: The product has the potential to contain undeclared almond slices.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 11, 2012· Toshiba American Medical Systems Inc

Recalled Item: Aplio 500/400/300 Diagnostic Ultrasound System (TUS-500/400/300). Device...

The Issue: Toshiba Medical Systems has received reports of startup issues with the...

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

Class II — Potential Health HazardOngoing
DrugDecember 10, 2012· Brower Enterprises Inc

Recalled Item: WOW Recalled by Brower Enterprises Inc Due to Undeclared Drug

The Issue: Marketed without an Approved NDA/ANDA: Brower Enterprises Inc., is recalling...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 10, 2012· Upsher Smith Laboratories, Inc.

Recalled Item: Divalproex Sodium Delayed-Release Tablets Recalled by Upsher Smith...

The Issue: Labeling: Label Error On Declared Strength; Some bottles of product were...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 10, 2012· Integra LifeSciences Corp.

Recalled Item: Integra XKnife¿ Stereotactic Radiosurgery and Radiotherapy Treatment...

The Issue: Depending on the system configuration, a software error message in versions...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2012· Becton Dickinson & Co.

Recalled Item: BBL(TM) Fildes Enrichment Recalled by Becton Dickinson & Co. Due to...

The Issue: Enrichment media intended to enhance the cultivation of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Flowtron Trio DVT Pump Recalled by Arjo, Inc. dba ArjoHuntleigh Due to The...

The Issue: The Flowtron Trio DVT Pump has been marketed without proper FDA Approval.

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

Class II — Potential Health HazardOngoing
DrugDecember 7, 2012· Bayer Healthcare, LLC

Recalled Item: Bronkaid Dual Action Formula Recalled by Bayer Healthcare, LLC Due to...

The Issue: Labeling: Label lacks warning or Rx legend; Certain information was...

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

Class III — Low RiskOngoing
Refund
DrugDecember 7, 2012· West-ward Pharmaceutical Corp.

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

The Issue: Presence of Foreign Substance: Uncharacteristic blacks spots on tablets.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2012· West-ward Pharmaceutical Corp.

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

The Issue: Presence of Foreign Substance: Uncharacteristic black spots identified as a...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2012· West-ward Pharmaceutical Corp.

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

The Issue: Presence of Foreign Substance: Uncharacteristic spots identified as steel...

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

Class II — Potential 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
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