Product Recalls in Utah

Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,818 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
1,818 in last 12 months

Showing 4184141860 of 49,677 recalls

DrugJune 6, 2014· Estee Lauder Inc

Recalled Item: DENBLAN Anticavity Fluoride Toothpaste Recalled by Estee Lauder Inc Due to...

The Issue: Stability Data Does Not Support Expiry

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

Class III — Low RiskOngoing
Refund
DrugJune 6, 2014· Hospira Inc.

Recalled Item: Heparin Sodium in 5% Dextrose Injection Recalled by Hospira Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 6, 2014· Green Smoothie Girl

Recalled Item: GreenSmoothieGirl TriOmega Superfood Recalled by Green Smoothie Girl Due to...

The Issue: The products contain Organic Sprouted Chia Powder that may be contaminated...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 5, 2014· Olde Thompson, Inc.

Recalled Item: Kirkland Signature Coarse Ground Malabar Pepper Recalled by Olde Thompson,...

The Issue: Olde Thompson is recalling Kirkland Signature Coarse Ground Malabar Black...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Exchange Kit Model Numbers 32001524 (24 cm) Recalled by Argon...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aqua 540 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Adaptor Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Humidifier Adaptor Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Peel Away Kit Recalled by Argon Medical Devices, Inc Due to...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak SW/EAU Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Chronic Hemodialysis Catheter Standard Kit Recalled by Argon...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Excelsior Medical Corp

Recalled Item: Excelsior Medical Sterile Triple Lead Tubing Set and Sterile Heavy Recalled...

The Issue: There is a potential for a leak. A molding defect in the connector that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee and Artis zeego systems. x-ray Recalled by Siemens Medical...

The Issue: There is a potential problem with Artis zee and Artis zeego systems running...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the respiratory gas humidifier adaptor packaging may be creased...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak SW/EAU Sterile Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing