All recall categories

Recalls distributed in Utah

These notices name Utah in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

2,860 stored notices name Utah, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Utah too — those are in the archive.

Medical devices

Reported Aug 10, 2022

The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Neotract Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

Merlin PCS 3650 programmer Model 3330 software

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

St. Jude Medical, Cardiac Rhythm Management Division

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 10, 2022

Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Procter & Gamble Company

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 10, 2022

Amaranth Grain Organic, brand Natural Grocers, packaged in plastic bag, net wt. 1 LB (454g) UPC 0 00080 12550 1. Label…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Vitamin Cottage Natural Food Markets, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 3, 2022

REF: 4P52-20 Hemoglobin A1c for use with Architect, IVD, CE, R1 1 x 52 mL, R2 1 x 20 mL, A1cDL 2 x 35 mL

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2022

Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large Clip Applier, Model 420327 Da Vinci S/Si…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Company

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

LifeGlobal Fast Freeze Thawing Kit, Model No. GFT5-055

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determination of…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

R & D Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

SX-One MicroKnife

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sonex Health LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Isopure Sodium Bicarbonate Mixing and Distribution System (IsoMix PRO)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Isopure Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

MiniMed 620G Insulin Pump (O.U.S. version)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Ventana HE 600 System, automated slide preparer, for use in laboratories.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ventana Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zeltiq Aesthetics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

Omnera 400T Digital Radiographic System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arcoma AB

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Covidien LLC

8 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 13, 2022

SoDelicious DairyFree Wondermilk Dairy Free Frozen Dessert Salted Caramel Sundae, 3 - 4 fl oz (12 fl oz) cones per…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Danone US LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 13, 2022

ABL800 Flex Analyzer Model Numbers 393-800 and 393-801

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2022

VOLISTA StandOP Surgical Light, Product Code/Part Numbers ARD568811901 VLT600SF AIM STP ARD568811911 VLT600SF AIM STP…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Getinge USA Sales Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2022

Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Volcano Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 29, 2022

Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Peach Mango Natural & Artificial Flavor, 33.8 FL OZ (1.05…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 29, 2022

Mini Peanut Butter Cream Pie. Product was available for purchase at the following banner: Haggen. Packaged in clear…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Albertsons Companies LLC

10 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 29, 2022

Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk, Soy, Wheat Dist. & Sold Exclusively By:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Taylor Farms Retail Inc.

FDA (openFDA food enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.