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. 1,670 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,670 in last 12 months

Showing 4212142140 of 47,632 recalls

FoodOctober 11, 2013· Metagenics, Inc.

Recalled Item: Spectrazyme Recalled by Metagenics, Inc. Due to Metagenics is recalling...

The Issue: Metagenics is recalling Spectrazyme because their raw material supplier...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 11, 2013· yoders country market

Recalled Item: Custom made gift boxes containing: HONEY ROASTED PEANUTS Recalled by yoders...

The Issue: Honey Roasted Peanuts, packaged in custom gift boxes, contained milk and...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi INSANE AMP'D Dietary Supplement capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi BTrim ULTIMATE BOOST Dietary Supplement capsules Recalled by Pure...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules Recalled by Pure...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi BTrim MAX Dietary Supplement capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi INSANE Bee Pollen Dietary Supplement Capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi AMP'D UP Advanced Weight Loss Dietary Supplement capsules Recalled...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 10, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Mixing Cup Arrays utilized on VITROS 250 Recalled...

The Issue: Ortho Clinical Diagnostics issued a product correction notification for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Mizuho America, Inc.

Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...

The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Nova Biomedical Corporation

Recalled Item: Nova StatStrip/StatSensor Hospital Blood Glucose Meter Recalled by Nova...

The Issue: Revised Battery Instructions for Removal and Expiration Date due to battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Mizuho America, Inc.

Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...

The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Biomet, Inc.

Recalled Item: Juggerknotless Drill Bit Recalled by Biomet, Inc. Due to Investigation...

The Issue: Investigation identified that the design of the drill bit may make the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: VariAx Compression Plating System Recalled by Stryker Howmedica Osteonics...

The Issue: Stryker received two reports indicating that during screw insertion under a...

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

Class II — Potential Health HazardOngoing
FoodOctober 10, 2013· Nutrition Center, Inc. dba Nutri-West

Recalled Item: Total Enzyme Recalled by Nutrition Center, Inc. dba Nutri-West Due to...

The Issue: Nutrition Center voluntarily recalled Total Enzymes and Total Probiotics...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2013· Nutrition Center, Inc. dba Nutri-West

Recalled Item: Total Probiotics Recalled by Nutrition Center, Inc. dba Nutri-West Due to...

The Issue: Nutrition Center voluntarily recalled Total Enzymes and Total Probiotics...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 9, 2013· Zimmer, Inc.

Recalled Item: Trinica Anterior Lumbar Plate (ALP) system Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Spine, Inc. is initiating a correction regarding the Trinica ALP...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS CA 125 II Calibrators For use in the calibration Recalled by...

The Issue: Ortho Clinical Diagnostics issued a Product Correction Notification for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2013· GE Healthcare, LLC

Recalled Item: GE Optima CT520 and Optima CT540 Computed Tomography (CT) systems. Recalled...

The Issue: There is an issue with the Manual Film Composer feature on some CT products....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2013· Arrow International Inc

Recalled Item: Arrow Transradial Artery Access products Arrow Transradial Artery Access...

The Issue: There is a risk that the introducer needles packaged within the kits can be...

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

Class II — Potential Health HazardOngoing