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. 2,507 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,507 in last 12 months

Showing 1894118960 of 28,579 recalls

Medical DeviceJanuary 4, 2017· Endologix

Recalled Item: AFX2 Endovascular AAA System Item No. Item Description F00820-01...

The Issue: Endologix updated information on the rates of Type III endoleaks and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2017· Stryker Leibinger GmbH & Co. KG

Recalled Item: 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design Recalled...

The Issue: An incorrect sterility status on the label, non-sterile products labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2017· Stryker Leibinger GmbH & Co. KG

Recalled Item: QUINTUBE Monitor Pack (5 tubes/pk Recalled by Stryker Leibinger GmbH & Co....

The Issue: An incorrect sterility status on the label, non-sterile products labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 1, 2017· BioMerieux SA

Recalled Item: Ceftriaxone TX 32 US S30 Recalled by BioMerieux SA Due to Potential...

The Issue: Potential performance issue on strain categorization.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 30, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Plum 360 Infusion Pump Recalled by Hospira Inc., A Pfizer Company Due to...

The Issue: Depleted Battery alarm shows instead of Replace Battery. On battery power,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes Radial Head Prosthesis System Recalled by Synthes (USA) Products LLC...

The Issue: There is the possibility that the radial stem may loosen post-operatively at...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 900-112: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 900-130: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 900-120: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120BT: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-110: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 900-115: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115BT: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Villa Sistemi Medicali S.P.A.

Recalled Item: Juno DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...

The Issue: Patient fell from the table because the footrest of the device detached from...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Immuno-Mycologics, Inc

Recalled Item: Cryptococcal Antigen Lateral Flow Assay (CrAg LFA) Recalled by...

The Issue: The affected products have approximately a 91% specificity while the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Endologix

Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...

The Issue: Endologix updated the Instructions for Use (IFU) and implemented...

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

Class II — Potential Health HazardOngoing