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 3446134480 of 49,677 recalls

FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 3/4" Yellow Onion Dice Recalled by Oregon Potato Company Due to...

The Issue: IQF 3/4" Frozen Yellow Onion Dice is voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 1/4" Frozen WHITE Onion Dice Recalled by Oregon Potato Company Due to...

The Issue: IQF 1/4" White Onion Dice is voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 1/4 x 1/4 Yellow Onion Dice Recalled by Oregon Potato Company Due to...

The Issue: 1/4 x 1/4 Frozen Yellow Onion Dice was voluntarily recalled because it has...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: 3/8" White Onion Strip-FRESH Recalled by Oregon Potato Company Due to...

The Issue: 3/8" White Onion Strip-FRESH was voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: 705000 IQF 3/8" Dice Yellow Onion Recalled by Oregon Potato Company Due to...

The Issue: 3/8" Frozen Yellow Onion Dice was voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 5, 2016· Empirical Laboratories, Incorporated

Recalled Item: Liposomal Magnesium Nutritional Supplement. 6 FL. OZ (180 ml) The Recalled...

The Issue: Empirical Labs is recalling Liposomal Magnesium because of the potential for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 5, 2016· Ceg Enterprises Llc

Recalled Item: Germ Terminator Recalled by Ceg Enterprises Llc Due to CEG Enterprises, LLC...

The Issue: CEG Enterprises, LLC is recalling Germ Terminator Toothbrush Sanitizer GT100...

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

Class II — Potential Health HazardOngoing
DrugApril 5, 2016· Fresenius Kabi USA, LLC

Recalled Item: Cisatracurium Besylate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Incorrect/ Undeclared Excipient: Firm is recalling product due to an...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 4, 2016· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril & Hydrochlorothiazide Tables Recalled by Lupin Pharmaceuticals...

The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Recalled by Merge Healthcare, Inc. Due to Cardio...

The Issue: Cardio study list does not show STAT studies without .

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: MasimoSET LNOP DCI adult SpO2 reusable sensor Recalled by Merge Healthcare,...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Hemo software. The firm name on the labeling is Merge Healthcare...

The Issue: Use of the software may show an incorrect value to the user when viewing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive software. Recalled by Merge Healthcare, Inc. Due...

The Issue: The versions allow images to be stored without pixel data, resulting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

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

The Issue: When taking measurements from images on the Cardio workstation or from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

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

The Issue: Potential exists for an incorrect patient image being displayed which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

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

The Issue: Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive (ICEA) software. iConnect Enterprise Archive is...

The Issue: The study is archived but cannot be opened in iConnect Access and cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station Import Utility (ESIU). The firm name on Recalled by Merge...

The Issue: System locks up which may result in potential patient injury or delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: MasimoSET LNOP DCIP pediatric/slender digit SpO2 reusable sensor Recalled by...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive (ICEA) software. The firm name on the Recalled...

The Issue: An error message can occur resulting in the prior studies being unavailable...

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

Class II — Potential Health HazardOngoing