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.
2,916 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.
Reported Mar 4, 2015
TDX Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 4, 2015
CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 25, 2015
Condies Foods, Bold & Zesty Salsa, 14 oz, UPC: 05077744220
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Condies Foods, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 25, 2015
Caramel Apples packaged in the following configurations with Best By date range - 8/25-11/23/2014, Responsible firm…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lochirco Fruit & Produce Inc.
7 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 25, 2015
Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use with the Robotic Arm Interactive Orthopedic System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Feb 25, 2015
MC-500 Multicolor Laser Photocoagulator; Indicated for use in retinal photocoagulation for treatment of ocular fundus…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Feb 25, 2015
Terumo HX2 Temperature Management System provides temperature control of two independent water circuits that directly…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Feb 18, 2015
Fruitful Juice Products Bloody Mary Beverage Concentrate with Jalapeno Flavor; Contains 59% Juice; 2 + 1 packed in 3…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Damon Industries
6 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 18, 2015
The MAYFIELD¿ Ultra 360 Base Unit for head positioner, one unit per package. Product Usage: This product provides the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corporation
FDA (openFDA device enforcement)
Reported Feb 18, 2015
MorningStar Farms Spicy Black Bean Burger: 9.50 oz (4 ct) - UPC 2898939207; 18.90 oz (8 ct): UPC 2898971750; 8.7 lb…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellogg USA Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 18, 2015
MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm; Part Number 86001; Lot Numbers A1405048, A1404026 Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Craniomaxillofacial Division
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 11, 2015
Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health
FDA (openFDA device enforcement)
Reported Feb 11, 2015
Dried Bean Curd Satay Flavor, 24x150g, Item No. 8533.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gemini Food Corporation Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 11, 2015
ABL90 FLEX analyzer; Model number 393-090. A portable, automated analyzer that measures pH, blood gases, electrolytes,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Feb 11, 2015
MobileDiagnost wDR motorized portable diagnostic X-ray systems.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal S.A.
FDA (openFDA device enforcement)
Reported Feb 4, 2015
The Revolution CT is a multi-slice (256 detector row) CT scanner consisting of a gantry, patient table, scanner desktop…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Feb 4, 2015
Syngo RT Therapist: The intended use of the SIEMENS branded ARTISTE, ONCOR and PRIMUS family of linear accelerator…
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)
Reported Feb 4, 2015
Thera Tablets with Beta Carotene Dietary Supplement
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Harvard Drug Group, LLC
FDA (openFDA food enforcement)
Reported Jan 29, 2015
California Firm Recalls Chicken Stew Products Produced Without Benefit of Import Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.California Firm
USDA FSIS
Reported Jan 28, 2015
Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 28, 2015
PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genetic Testing Institute,Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument software versions since…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia US Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging Cradles are designed to be used with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
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.