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 48,123 notices were distributed nationwide, so they reach Utah too — those are in the archive.

Medical devices

Reported Aug 27, 2014

Gyrus ACMI Falope-Ring Dilator, item 000878-4. The Falope-Ring Dilator is a conical plastic device that is a component…

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

Gyrus Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2014

All brochures printed before November 20, 2013 for the HyperBlue 1530 medical laser, including the product brochure and…

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

Hyperion Medical

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2014

Philips IP5 Information Portal The Expression Information Portal (Model IP5), a display and device controller for…

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2014

TomoTherapy Treatment System, Model: Hi-Art, Catalog/Part Number: H-0000-0003, software versions 1.2.0, 1.2.1 and 1.2.2…

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

TomoTherapy Incorporated

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2014

Gelweave (TM) Vascular Prostheses Manufactured by - VASCUTEK Ltd a TERUMO company

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

Vascutek, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Esaote PA230E Transducer A portable and cart base ultrasound system for general and cardiovascular imaging

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

Biosound Esaote, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Codman Certas - In Line Valve Only; Product Code: 82-8800 The Codman Certas Programmable valve is an implantable device…

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

Codman & Shurtleff, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Medtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Catheter Pump Segment Revision…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 13, 2014

Sonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2014

Medtronic Nexdrive Micropositioning Drive. Models Ml-1000 and Ml-2000. For use in conjunction with the Medtronic…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2014

MC-500 Multicolor Laser Photocoagulator; Distributed by NIDEK Inc. Manufactured by NIDEK CO., Ltd, Japan. For use in…

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

Nidek Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2014

InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.

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

Stryker Medical Division

FDA (openFDA device enforcement)

Food

Reported Aug 6, 2014

Original Silk Light Soymilk Half Gallon, Distributed by WhiteWave Foods Broomfield, Colorado 80021, UPC 0 25293 60101 7

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

White Wave Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 30, 2014

RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the…

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

DePuy Orthopaedics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2014

MK5 NX Controller--Wheelchair controller

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

Invacare Corporation

FDA (openFDA device enforcement)

Food

Reported Jul 30, 2014

Fat free cottage cheese sold under the Knudsen or Kraft brand and packaged in a plastic container with a net weight of…

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

Kraft Foods Group

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 30, 2014

QLAB 10 Core Module PN 453561704771. QLAB Quantification Software is a software application package designed to view…

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

Philips Ultrasound, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2014

Sarns D4 Aortic Arch Cannulae 6.0mm, 7mm & 8mm angled and straight tip with or without side holes and/or luer Product…

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

Terumo Cardiovascular Systems Corporation

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2014

Titan T 5K Motor Product Usage: Low-speed motor is used with various attachments to perform a variety of dental…

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

Dental EZ Group Star Dental Division

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2014

ACL TOP (Base), automated coagulation laboratory instrument.

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

Instrumentation Laboratory Co.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2014

e.cam camera system. Emission Computed Tomography System used to detect or image the distribution of radionuclides in…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2014

Certified Organic, Owl Canyon Whole Eggs, packed in one dozen and half-dozen cardstock packages, with a packing date of…

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

Six Dog, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 16, 2014

HLD System, Model 610, Medical Device Cleaning and High Level Disinfection Washer/Pasteurizer.

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

Cenorin, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2014

Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.

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

Karl Storz Endoscopy

FDA (openFDA device 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.