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.

2,917 stored notices name Utah, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Utah too — those are in the archive.

Medical devices

Reported Aug 23, 2017

Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…

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

Cyberonics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 23, 2017

Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,

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

NatureAll-STF Holding, LLC

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 16, 2017

Syringe Bulb, 60 CC 50 pcs per case. The products are used to inject fluids into, or withdraw fluids from the body.…

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

International Medsurg Connection, Inc.

58 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 9, 2017

Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in white plastic…

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

Professional Complementary Health Formulas, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 9, 2017

Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2017

STOCKERT Heater-Cooler System 3T, 230 V

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

Sorin Group USA, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 26, 2017

Agfa Healthcare NX 3.0.8950 Imaging Processing Software

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

AGFA Healthcare Corp.

FDA (openFDA device enforcement)

Food

Reported Jul 26, 2017

FIT&FOCUSED SUPPLEMENTS CLA 3000mg CONJUGATED LINOLEIC ACID LEAN BODY FORUMLA 135 SOFTGELS; UPC: 7 28028 44036 2

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

Fit and Focused Supplements

FDA (openFDA food enforcement)

Food

Reported Jul 26, 2017

Futaba Sesame Hijiki Rice Seasoning; 2.29 oz. glass jar; 4 902533 023173

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

J F C International Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 26, 2017

Penumbra 3D Revascularization Device It is indicated for used in the revascularization of patients with acute ischemic…

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

Penumbra Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 19, 2017

Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Jul 19, 2017

Simple truth Dry Roasted Macadamia Nuts 12 oz bags UPC 0 1111 00247 8 DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO…

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

Kroger Corporate Food Technology Laboratory

FDA (openFDA food enforcement)

Food

Reported Jul 19, 2017

AMERICAS CHOICE B/D SHRIMP BEER BATTERED POPCORN 12/14 OZ

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

National Fish & Seafood, Inc.

32 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 19, 2017

The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended for cleaning and high-level disinfection of…

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

Natus Medical Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Jul 19, 2017

Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive…

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

Natus Neurology Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 19, 2017

ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI…

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

Oscor, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 19, 2017

Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and…

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

Pentax

FDA (openFDA device enforcement)

Food

Reported Jul 12, 2017

Chili Pequino 0.25 oz packaged in a clear plastic bag; Product Code 10106

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

Bolner's Fiesta Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 12, 2017

3DKNEE(TM) SYSTEM e+, tibial Insert, LEFT Sz 6 / 11mm, REF 391-11-706, QTY 01, The 3DKnee Insert HXL Tibial Inserts are…

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

Encore Medical, LP

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 12, 2017

Nussloch GmbH ASP6025 Tissue Processor

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 28, 2017

PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE PASTE NET WT 4 OZ (113g) UPC 0 11110 80699 4…

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

Monfitello

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 28, 2017

Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…

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

Vascular Solutions, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 21, 2017

Western Family Onion Soup Mix, 2.25 oz. pouches packaged in 4.5-oz. cartons

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

Gilster-Mary Lee Corp.

FDA (openFDA food enforcement)

Free recall alerts

Get alerted about new Utah recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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.