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 4538145400 of 47,632 recalls

DrugNovember 8, 2012· Hospira Inc.

Recalled Item: Carboplatin Injection Recalled by Hospira Inc. Due to Crystallization:...

The Issue: Crystallization: Product is being recalled due to visible particulates...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 8, 2012· Hospira Inc.

Recalled Item: Carboplatin Injection Recalled by Hospira Inc. Due to Crystallization:...

The Issue: Crystallization: Product is being recalled due to visible particulates...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 8, 2012· Procter & Gamble Co

Recalled Item: Vicks NyQuil Cold & Flu Recalled by Procter & Gamble Co Due to Labeling...

The Issue: Labeling Illegible: Portions of the product labeling in the area of the...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 8, 2012· Whole Foods Market

Recalled Item: Whole Foods Market Panettone Chocolate - 26.4 oz Recalled by Whole Foods...

The Issue: The reason for the recall was that a small portion of the Whole Foods Market...

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

Class III — Low RiskOngoing
Refund
FoodNovember 8, 2012· Nestle USA

Recalled Item: Nesquik Chocolate Powder Recalled by Nestle USA Due to Potential Salmonella...

The Issue: Nestle is recalling Nesquik Chocolate Powder because certain lots of its...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 8, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: ShapeMatch Cutting Guides Product Usage: The ShapeMatch Cutting Guides are...

The Issue: With regards to ShapeMatch Cutting Guides using MRI Imaging, Stryker...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 8, 2012· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Infinix-i X-Ray System. A radiographic and fluoroscopic x-ray system...

The Issue: Lost and incorrect images. When using the "F-Rec" fluoroscopy image...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2012· Medline Industries Inc

Recalled Item: Medline Angio Drape Pack Radiology-LF Recalled by Medline Industries Inc Due...

The Issue: The non-sterile Waste Bag component in the custom pack was attached to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2012· MOOG Medical Devices Group

Recalled Item: EnteraLite Infinity Enteral Feeding Pump identified with the following list...

The Issue: MOOG Medical Devices Group is conducting a voluntary for a limited set of...

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

Class II — Potential Health HazardOngoing
FoodNovember 7, 2012· Reaction Nutrition LLC

Recalled Item: Clinical LIVE Dietary Supplement Immune Support 694.325 mg 90 capsules...

The Issue: The product contained an undeclared allergen, Colostrum, which is considered...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 7, 2012· Fresh Express Incorporated

Recalled Item: Fresh Express brand Recalled by Fresh Express Incorporated Due to Potential...

The Issue: Product tested positive for Salmonella

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 8 X80MM Tl Product Recalled by DePuy Spine,...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 10 X 80MM Tl Recalled by DePuy Spine, Inc....

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 8 X100MM Tl Product Recalled by DePuy...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 8 X70MM Tl Product Recalled by DePuy Spine,...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 10X100MM Tl Product Code: Recalled by DePuy...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 9 X 80MM Tl Recalled by DePuy Spine, Inc....

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 9 X100MM Tl Product Recalled by DePuy...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 9 X70MM Tl Product Recalled by DePuy Spine,...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 10 X 70MM Tl Recalled by DePuy Spine, Inc....

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing