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. 2,259 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,259 in last 12 months

Showing 4604146060 of 47,632 recalls

DrugAugust 14, 2012· Bracco Diagnostic Inc

Recalled Item: Choletec - Kit for the Preparation of Technetium Tc 99m Mebrofenin Recalled...

The Issue: Presence of Particulate Matter; potential for charcoal particulates

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

Class III — Low RiskOngoing
Refund
DrugAugust 14, 2012· Actavis Mid Atlantic LLC

Recalled Item: Prometh VC Plain Recalled by Actavis Mid Atlantic LLC Due to...

The Issue: Impurities/Degradation Products: Recalled lots do not meet room temperature...

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

Class III — Low RiskOngoing
Refund
DrugAugust 14, 2012· Actavis Mid Atlantic LLC

Recalled Item: Prometh VC with Codeine Cough Syrup Recalled by Actavis Mid Atlantic LLC Due...

The Issue: Impurities/Degradation Products: Recalled lots do not meet room temperature...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 14, 2012· Lansinoh Laboratories Inc

Recalled Item: THERA PEARL 3-in-1 BREAST THERAPY Recalled by Lansinoh Laboratories Inc Due...

The Issue: The Spanish translation on the Instructions for Use (IFU) insert and product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2012· Biomet, Inc.

Recalled Item: JUGGERKNOT IN¿GUIDE PUNCH Recalled by Biomet, Inc. Due to Investigation...

The Issue: Investigation found that the current design of the product allows the...

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

Class II — Potential Health HazardOngoing
FoodAugust 13, 2012· Drucker Labs LP

Recalled Item: intraKID Lot 658 with a Best By date of 12/12 Recalled by Drucker Labs LP...

The Issue: After extensive testing and investigation, Drucker Labs has determined that...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 13, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare became...

The Issue: GE Healthcare became aware of a potential issue related to incorrect image...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: Mindray A5 Anesthesia Delivery System Manufactured in China for Mindray...

The Issue: Mindray has identified the potential for a system leak resulting an issue...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 13, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: Mindray A3 Anesthesia Delivery System Manufactured in China for Mindray...

The Issue: Mindray has identified the potential for a system leak resulting an issue...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 13, 2012· Vital Images, Inc.

Recalled Item: Software for Vitrea Recalled by Vital Images, Inc. Due to Vital Images has...

The Issue: Vital Images has found two potential errors in calcium score values in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2012· Neomend Inc

Recalled Item: Progel Pleural Air Leak Sealant Recalled by Neomend Inc Due to Product was...

The Issue: Product was distributed with an incorrect expiration date. Product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS N-Mid¿ Osteocalcin Recalled by Immunodiagnostics Systems Ltd Due to...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS Urine BETA CrossLaps ELISA Recalled by Immunodiagnostics Systems Ltd Due...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Control Set Recalled by...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS Intact PINP Control Set Recalled by Immunodiagnostics Systems Ltd...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS Intact PINP Recalled by Immunodiagnostics Systems Ltd Due to It has...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS N-Mid¿ Osteocalcin Recalled by Immunodiagnostics Systems Ltd Due to...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Recalled by...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Capsule Tech Inc.

Recalled Item: Capsule Neuron Docking Station Recalled by Capsule Tech Inc. Due to Capsule...

The Issue: Capsule Neuron Docking Station may experience a lost connection, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Steris Corporation

Recalled Item: QKC1692E The QKC1692E Quick Connect device connects endoscopes to the...

The Issue: STERIS has been actively seeking devices for quick connect revalidation...

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

Class II — Potential Health HazardOngoing