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. 2,349 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,349 in last 12 months

Showing 2690126920 of 47,632 recalls

Medical DeviceAugust 21, 2017· Beckman Coulter Inc.

Recalled Item: AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer Recalled by...

The Issue: Beckman Coulter has identified that an incorrect setting using a proprietary...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Picture Archiving and Communication System (PACS) with software...

The Issue: Software update to correct several issues that include (1)Potential data...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Philips Electronics North America Corporation

Recalled Item: Azurion 3 M12 Recalled by Philips Electronics North America Corporation Due...

The Issue: When using the downscale option with the Allura R9 system or Azurion R1.1...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Olympus Corporation of the Americas

Recalled Item: A20975A "Working insert Recalled by Olympus Corporation of the Americas Due...

The Issue: Olympus has received complaints about fragments of adhesive which detached...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Invivo Corporation

Recalled Item: Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive...

The Issue: Intermittent communication between the host system and the FlexCardio

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

Class II — Potential Health HazardOngoing
DrugAugust 18, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Paroxetine tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Presence of Foreign tablets/capsules: risperidone Tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 18, 2017· Integra LifeSciences Corp.

Recalled Item: TCC-EZ Recalled by Integra LifeSciences Corp. Due to A quarantined lot of...

The Issue: A quarantined lot of the devices was released for sale. Devices from this...

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

Class II — Potential Health HazardOngoing
DrugAugust 17, 2017· VistaPharm, Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution 7.5 mg/325 mg per...

The Issue: Labeling: Not Elsewhere Classified; product is incorrectly labeled as Class...

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

Class III — Low RiskOngoing
Refund
DrugAugust 17, 2017· Vital Rx, Inc. dba Atlantic Pharmacy and Compounding

Recalled Item: All Sterile Products within expiry Recalled by Vital Rx, Inc. dba Atlantic...

The Issue: Lack of Assurance of Sterility .

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: BevaDex (bevacizumab) 0.06mL Prefilled 32 g (1.25mg/1mg) Syringes Recalled...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Mannitol 20% Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: PF-Glutathione 200mg/ml Recalled by Bella Pharmaceuticals, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Bevacizumab Prefilled 30g and 31 gram 1.25mg/0.05mL Syringes Recalled by...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: B-Complex Recalled by Bella Pharmaceuticals, Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Fluorescein Sodium Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: L-Glutamine 100mg Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Sodium Bicarbonate 8.4% Recalled by Bella Pharmaceuticals, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Phenylephrine2.5%/Tropicamide 1% Ophthalmic Solution Recalled by Bella...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Calcium chloride 10% Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: G.A.C 25/100/250mg Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund