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. 1,760 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,760 in last 12 months

Showing 3142131440 of 47,632 recalls

FoodAugust 9, 2016· Rabbit Creek Products Inc.

Recalled Item: Lemon Blueberry Quick Bread Mix Recalled by Rabbit Creek Products Inc. Due...

The Issue: Bread, muffin, and brownie mixes may have been manufactured with flour...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 9, 2016· Rabbit Creek Products Inc.

Recalled Item: Flower Pot Pumpkin & Cream Cheese Quick Bread Mix Recalled by Rabbit Creek...

The Issue: Bread, muffin, and brownie mixes may have been manufactured with flour...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 9, 2016· Rabbit Creek Products Inc.

Recalled Item: Blooming Onion Beer Bread Mix Recalled by Rabbit Creek Products Inc. Due to...

The Issue: Bread, muffin, and brownie mixes may have been manufactured with flour...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 9, 2016· Rabbit Creek Products Inc.

Recalled Item: Bombshell Brownie Mix (Gooey Brownie w/Caramel Fudge Icing) Recalled by...

The Issue: Bread, muffin, and brownie mixes may have been manufactured with flour...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 9, 2016· Swissray Medical

Recalled Item: ddR Formula B X-ray System Recalled by Swissray Medical Due to Possible...

The Issue: Possible injury due to movement of the arm, calibration loss and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Becton Dickinson & Company

Recalled Item: BD 23 G x .75 in. BD Vacutainer¿ Push Button Recalled by Becton Dickinson &...

The Issue: BD has received multiple reports of units associated with the 23 G x .75 in....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur¿ Calibrator U Recalled by Siemens Healthcare...

The Issue: Failure of analytical sensitivity with Calibrator U kit lots ending in 63...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· CareFusion 303, Inc.

Recalled Item: Alaris Syringe Module Model 8110 with software version 9.15 The Recalled by...

The Issue: A software anomaly with the Alaris Syringe module software version 9.15 may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Arrow International Inc

Recalled Item: Arterial Line Catheterization Kit with Sharps Safety Features Permits access...

The Issue: Shipping carton labeling error.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Permits access...

The Issue: Shipping carton labeling error.

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

Class II — Potential Health HazardOngoing
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Ninjacof-A (acetaminophen Recalled by Pharmatech LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Diocto Syrup (docusate sodium) Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Sennazon (sennosides) Syrup Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Aller-Chlor (chlorpheniramine maleate) Syrup Recalled by Pharmatech LLC Due...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Ninjacof (chlophedianol HCl and pyrilamine maleate) Liquid Recalled by...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Senexon Liquid (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Senna Syrup (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2016· Teva North America

Recalled Item: Claravis (isotretinoin capsules USP) Recalled by Teva North America Due to...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via picture archiving and communication system Syngo via is a Recalled...

The Issue: Software error. Incorrect values for the volume calculation from a freehand...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Medtronic Inc.

Recalled Item: CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic...

The Issue: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software...

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

Class II — Potential Health HazardOngoing