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.

Food

Reported Feb 8, 2023

Inositol packaged in white plastic bottle with UPC 4065111562 and labeled in part, "***PROFESSIONAL FORMULAS…

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

Professional Complementary Health Formulas, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 8, 2023

SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000

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

SynCardia Systems LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation

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

Teleflex LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2023

BD Pyxis MedBank System - Product Label/labeling pending

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 18, 2023

Martinelli's Gold Medal Apple Juice 1 liter (33.8 oz.) glass bottle UPC: 4124400102 6 Bottles per bundled…

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

S Martinelli & Company

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2023

VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD…

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

Ventana Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 4, 2023

Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…

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

Acumed LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 4, 2023

XO Marshmallow Limited Edition: Banana Puddin' OMG (Ooey Marshmallow Goodness), 12oz. marshmallow fluff, 4 12oz. retail…

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

XO Marshmallow, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 28, 2022

X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.

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

NuVasive Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 28, 2022

Red Button Vintage Creamery French Silk Pie, Net Wt. 31.88 oz. (904g), in a clear plastic dome and black plastic base,…

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

Rocky Mountain Pies, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2022

Small Joint OATS Set, REF AR-8981-06S, 6mm; and Small Joint OATS Set, REF AR-8981-08S, 8mm, both containing a…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2022

2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors…

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

Bunnell, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 14, 2022

Enoki Mushroom Net wt. 200g (7.05 oz.) 25 units per case UPC: 16430-69080 Keep refrigerated Product of Korea

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

Green Day Produce

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2022

Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044

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

Intersect ENT, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 14, 2022

Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 tubs per case

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

Nestle-USA, Inc. (Corporate Office)

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2022

The FAST System and the FAST PBC Prep Cartridge together are a closed, rapid and automated sample preparation system…

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

Qvella Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2022

IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic use with the IMMULITE and IMMULITE 1000…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

Alcon Custom Pak Surgical Procedure Pack

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

Alcon Research, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

GREER M. FAENI, 0.25 mL 20 MG/ML, Item: K6, Analyte Specific Reagent, HYPERSENSITIVITY PNEUMONITIS test system, gel…

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

Greer Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

INTUITIVE Da Vinci Xi 8mm SureForm 30 Curved-Tip Stapler Da Vinci Xi|X REF 488530 INTUITIVE Da Vinci 8mm SureForm 30…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography (CT) system, software version 2.1.1

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

Mobius Imaging, LLC

FDA (openFDA device enforcement)

Food

Reported Nov 23, 2022

Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case

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

Abbott Laboratories

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 23, 2022

Superion¿ Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Food

Reported Nov 23, 2022

Gem City Fine Foods GF Flourless Chocolate Torte, 4 oz., frozen gluten free dessert, clear plastic package, UPC…

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

Gem City Fine Foods, LLC

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.