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. 2,346 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,346 in last 12 months

Showing 3158131600 of 47,632 recalls

FoodJuly 14, 2016· Monogram Appetizers, Inc

Recalled Item: Poppers brand Mozzarella Cheese Sticks Net Wt. 32 oz. (2 Recalled by...

The Issue: Monogram Appetizers is recalling Poppers Brand Mozzarella Cheese Sticks...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 14, 2016· Merge Healthcare, Inc.

Recalled Item: Merge RadSuite Recalled by Merge Healthcare, Inc. Due to It was reported by...

The Issue: It was reported by a customer that RadSuite images are not appearing as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Field failures were...

The Issue: Field failures were reported related to the da Vinci Xi Surgical System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Intuitive Surgical, Inc.

Recalled Item: STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field failures were...

The Issue: Field failures were reported related to the da Vinci Xi Surgical System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Intuitive Surgical, Inc.

Recalled Item: CURVED-TIP STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field...

The Issue: Field failures were reported related to the da Vinci Xi Surgical System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Straumann Manufacturing, Inc.

Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...

The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Straumann Manufacturing, Inc.

Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...

The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Estradiol Reagent Pack Recalled by...

The Issue: Ortho Clinical Diagnostics has issued a recall of their VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Diasorin Inc.

Recalled Item: LIAISON Estradiol II Gen Recalled by Diasorin Inc. Due to DiaSorin is...

The Issue: DiaSorin is issuing an urgent medical device correction for the LIAISON¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM Recalled by Siemens Medical...

The Issue: The possibility exists for contaminants, in the form of biomass, to develop...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS ZEE AND ZEEGO Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: The possibility exists for contaminants, in the form of biomass, to develop...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Recalled by Siemens Medical Solutions...

The Issue: The possibility exists for contaminants, in the form of biomass, to develop...

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

Class II — Potential Health HazardOngoing
DrugJuly 12, 2016· Supernus Pharmaceuticals, Inc.

Recalled Item: Trokendi XR (topiramate) extended-release capsule Recalled by Supernus...

The Issue: Superpotent Drug: Failure of assay specifications in the capsule.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2016· McCain Foods USA

Recalled Item: Breaded stuffed Jalapenos poppers labeled in part: Anchor breaded Fiesta...

The Issue: Firm used Flour from General Mills that has been contaminated with E. Coli O121.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2016· McCain Foods USA

Recalled Item: Fire roasted Poblano & Jalapeno popper bites packaged in a Recalled by...

The Issue: Firm used Flour from General Mills that has been contaminated with E. Coli O121.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 12, 2016· ELITech Group B.V.

Recalled Item: Viva-ProE Systems Recalled by ELITech Group B.V. Due to Software...

The Issue: Software malfunction; The action being taken due to the device becoming...

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2016· Mckesson Medical Imaging Group

Recalled Item: McKesson Radiology Recalled by Mckesson Medical Imaging Group Due to The...

The Issue: The STAT priority icon was not displayed in the Study List when the study...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2016· Resmed Corporation

Recalled Item: Quattro Air FFM MED  AMER Recalled by Resmed Corporation Due to Masks in...

The Issue: Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size...

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

Class II — Potential Health HazardOngoing
DrugJuly 11, 2016· Actavis Inc

Recalled Item: Dextroamphetamine Sulfate Extended-Release Capsules Recalled by Actavis Inc...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2016· General Mills, Inc

Recalled Item: Betty Crocker Delights Super Moist Party Rainbow Chip Cake Mix Recalled by...

The Issue: Three flavors of Betty Crocker cake mix are being recalled by General Mills...

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

Class I — Serious Health HazardOngoing
Refund