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 Oct 12, 2022

MR Patient Care Portal 5000 (Desktop Unit), Model Number 453564792561 This is a component of product number 866162.

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 12, 2022

Philips Respironics Amara View Minimal Contact Full-Face Mask

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

Philips Respironics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 12, 2022

WFM 365 Organic Creamy Caesar, 12oz, UPC#: 99482490029, Keep Refrigerated. Bottled in USA. Distributed by: Whole Foods…

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

Vanlaw Food Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 5, 2022

BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

Ambra PACS, Ambra ProViewer. Software for use as a primary diagnostic and analysis tool for diagnostic images.

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

DICOM Grid, Inc. d/b/a Ambra Health

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner…

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

MEDLINE INDUSTRIES, LP - Northfield

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

t:slim X2 insulin pump; t:slim X2 insulin pump with Dexcom G5; t:slim X2 insulin pump with Basal-IQ technology; t: slim…

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

Tandem Diabetes Care Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 5, 2022

Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 LB 1.7 OZ (502g) UPC code 0-45255-15221-0 Distributed by World…

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

World Variety Produce Inc. dba Melissa's

FDA (openFDA food enforcement)

Medical devices

Reported Sep 28, 2022

BD MaxGuard Extension Set with 4-way stopcock, REF: M4058

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

Carefusion

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2022

MicroClave Clear Neutral Connector. A bidirectional connector used as an accessory to an intravascular catheter placed…

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

ICU Medical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2022

Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within…

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

Steris Corporation Hopkins Facility

FDA (openFDA device enforcement)

Food

Reported Sep 21, 2022

The GFB Gluten Free Bites Dark Chocolate and Coconut 1.2oz. UPC 856818008895, 10 retail units per tray, 6 trays per…

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

West Thomas Partners, LLC. dba Gluten Free Bar

FDA (openFDA food enforcement)

Medical devices

Reported Sep 14, 2022

Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY…

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

ICU Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 7, 2022

Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ.…

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

Family Dollar Stores, Llc.

5 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 7, 2022

Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.

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

Oculus Optikgeraete GmbH

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…

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

Medtronic Neuromodulation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144

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

Mizuho OSI

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

Nobel Biocare N1 TiUltra TCC NP 3.5x13mm

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

Nobel Biocare

FDA (openFDA device enforcement)

Food

Reported Aug 24, 2022

Kabobs The Hors d'oeuvre Specialist TOMATO, BASIL & MASCARPONE ARANCINI 180 COUNT Prepared by: Kabobs, Inc., 5423 North…

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

Kabobs Acquisition Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 24, 2022

Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.

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

Myolyn Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 24, 2022

Sweet Loren's Place and Bake Sugar Cookie Dough, Net Wt. 12 oz.

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

Sweet Loren's

FDA (openFDA food enforcement)

Food

Reported Aug 17, 2022

Clear American brand "Strawberry Punch Snow Cone" flavored sparkling water beverage with other natural flavors; 1-liter…

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

Refresco Beverages US Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 17, 2022

cobas e801 Immunoassay Analyzer

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10

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

Aesculap Implant Systems LLC

1 more product in this recall

FDA (openFDA device 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.