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. 2,375 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,375 in last 12 months

Showing 4306143080 of 49,677 recalls

Medical DeviceJanuary 30, 2014· KCI USA, INC.

Recalled Item: PRE2055: Prevena Customizable Dressing 5-Pack Product Usage: The Prevena...

The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· KCI USA, INC.

Recalled Item: PRE1055: Prevena Dressing Recalled by KCI USA, INC. Due to Prevena...

The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· KCI USA, INC.

Recalled Item: PRE2055US: Prevena Customizable Dressing 5-Pack (US-ONLY) Product Usage: The...

The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· KCI USA, INC.

Recalled Item: PRE2001: Prevena Incision Management Customizable System Box Product Usage:...

The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· KCI USA, INC.

Recalled Item: PRE1001: Prevena Peel and Place System Kit Product Usage: The Recalled by...

The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· KCI USA, INC.

Recalled Item: PRE2001US: Prevena Incision Management Customizable System Box (US-ONLY)...

The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· KCI USA, INC.

Recalled Item: PRE1055US: Prevena Dressing Recalled by KCI USA, INC. Due to Prevena...

The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Select CAP Arterial Cannulae. Non-Vented Recalled by Medtronic...

The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....

The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....

The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Intersept Custom Tubing Pack which contain Select 3D or Recalled...

The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....

The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2014· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Select CAP Arterial Cannulae. Vented Recalled by Medtronic Inc....

The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...

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

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2014· Pfizer Inc.

Recalled Item: GREENSTONE BRAND fluconazole for Oral Suspension Recalled by Pfizer Inc. Due...

The Issue: Defective Container: Tamper evident ring failures discovered on some bottles.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2014· Fougera Pharmaceuticals Inc.

Recalled Item: Triamcinolone Acetonide Cream USP Recalled by Fougera Pharmaceuticals Inc....

The Issue: Labeling: Label Error on Declared Strength: There is a misprint on the end...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2014· Caraco Pharmaceutical Laboratories Ltd.

Recalled Item: Oxcarbazepine Tablets Recalled by Caraco Pharmaceutical Laboratories Ltd....

The Issue: Failed Tablet Specifications: Broken Tablets Present.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 29, 2014· Gano Excel USA Inc

Recalled Item: Gano C'Real Spirulina Recalled by Gano Excel USA Inc Due to Undeclared Wheat

The Issue: Gano Excel USA is recalling the C'Real Spirulina because it contains...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 29, 2014· Implantech Associates Inc

Recalled Item: Gelzone Shoulder Sleeve Recalled by Implantech Associates Inc Due to...

The Issue: Implantech initiated the voluntary recall of Gelzone Shoulder Sleever,...

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

Class II — Potential Health HazardOngoing
DrugJanuary 28, 2014· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Carisoprodol Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurity/degradation Specification

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

Class III — Low RiskOngoing
Refund
DrugJanuary 28, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Metformin HCl Extended-Release Tablets Recalled by Caraco Pharmaceutical...

The Issue: Presence of Foreign Tablet; customer complaint of some tablets of Gabapentin...

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

Class II — Potential Health HazardOngoing
Refund