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. 2,433 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,433 in last 12 months

Showing 3502135040 of 49,677 recalls

Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Deerfield Imaging

Recalled Item: Intra operative MRI Systems: Neuro II-SE Recalled by Deerfield Imaging Due...

The Issue: Emergency helium venting lines (i.e. quench lines) may not have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Ultra 8 IAB: 8Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: RediGuard IAB: 7Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: UltraFlex IAB: 7.5Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is Recalled by Arrow...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: UltraFlex IAB: 7.5Fr 40cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc.,...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
DrugFebruary 9, 2016· Alcon Research, Ltd.

Recalled Item: TEARS Naturale FREE (dextran 70 and hypromellose 2910) lubricant eye drops...

The Issue: Lack of Assurance of Sterility: Some single-use vials may be filled with...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 9, 2016· Urban Oven, LLC

Recalled Item: Urban Oven Artisan-Baked Short Bread Cookies Classic Butter All Natural...

The Issue: Urban Oven, LLC is recalling Urban Oven Butter Cookies, Cocoa Cookies, Pecan...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 9, 2016· Urban Oven, LLC

Recalled Item: Urban Oven Artisan-Baked Short Bread Cookies Pecan All Natural NET. Recalled...

The Issue: Urban Oven, LLC is recalling Urban Oven Butter Cookies, Cocoa Cookies, Pecan...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 9, 2016· Urban Oven, LLC

Recalled Item: Urban Oven Artisan-Baked Short Bread Cookies Lemon Pistachio All Natural...

The Issue: Urban Oven, LLC is recalling Urban Oven Butter Cookies, Cocoa Cookies, Pecan...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 9, 2016· Urban Oven, LLC

Recalled Item: Urban Oven Artisan-Baked Short Bread Cookies Cocoa All Natural NET Recalled...

The Issue: Urban Oven, LLC is recalling Urban Oven Butter Cookies, Cocoa Cookies, Pecan...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 9, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...

The Issue: A report can be confirmed with the incorrect patient demographics resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2016· Bard Peripheral Vascular Inc

Recalled Item: Denali Filter-Femoral Delivery System Product Code: DL900F/DL950F Recalled...

The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2016· Bard Peripheral Vascular Inc

Recalled Item: Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J...

The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...

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

Class II — Potential Health HazardOngoing