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 48,122 notices were distributed nationwide, so they reach Utah too — those are in the archive.
Reported Nov 30, 2016
COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Organic Cacao Nibs, packaged in 200g (7.05 oz) brown bags, UPC code 661594002032
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Level Ground Trading Limited
FDA (openFDA food enforcement)
Reported Nov 30, 2016
Fluid Management Set. Catalog Number K08-MP5159A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Philips Healthcare System X-ray Tomography Computed :
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Access Ostase Calibrators, Catalog No. 37305, B83876 Product Usage: The Access Ostase Calibrators are intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Brilliance iCT Computed Tomography X-ray system, Model 728306
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Philips Medical Systems (Cleveland) Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2016
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Dorothy Lynch Homestyle 8 oz., 16 oz., and 32 oz. bottles (12/case) and 128 oz. bottles (4/case)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tasty Toppings Inc.
FDA (openFDA food enforcement)
Reported Nov 16, 2016
Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
DM Light Slices Yellow Cling Peaches -15 oz (425g) 300 x 407
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Monte Research Center - Walnut Creek
FDA (openFDA food enforcement)
Reported Nov 2, 2016
4205 Journey Rolling Walker Product Usage: used to assist people in walking
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nova Ortho-Med Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US, ex-tem. Used to monitor the coagulation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TEM Systems Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Awareness Corporation
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Cut Green Beans packed under brand names of: Allens Cut Green Beans (Ejotes Cortados Lago Azul) Blue Lake . Allens…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Del Monte Research Center - Walnut Creek
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2016
HeartWare Ventricular Assist System Controller Product Usage: For use as a bridge-to-cardiac transplantation in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Nature's One, Organic PediaSmart¿ Dairy Vanilla complete nutrition beverage for kids 1 to 13 years NET WT 12.7 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Oct 26, 2016
OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Oct 26, 2016
25 gauge VersaVit 2.0 Core Essentials Procedure Pack, Product/Part Number 70025E, packaged in HIPS rigid tray with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synergetics Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 19, 2016
The Introes Pocket Bougie is an endotracheal tube introducer. The device is an endotracheal tube introducer and it is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brathwaites Oliver Medical
FDA (openFDA device enforcement)
Reported Oct 19, 2016
CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter, REF/Catalog Number CS-023, STERILE, Rx Only Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
FDA (openFDA device enforcement)
Reported Oct 19, 2016
OEC Brivo 715 Prime, OEC Brivo 785 Essential, OEC Brivo 865 Advance Product Usage: The OEC Brivo Mobile C-Arm X-Ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Oct 19, 2016
HeartWare Ventricular Assist System (HVAD), US product: Model No.: 1103; and International Product: Model No.: 1104XX.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare, Inc.
FDA (openFDA device enforcement)
Reported Oct 19, 2016
Phoenix Recon Soft Tissue Sleeve Guide, Surgical, Instrument for the sleeve and Orthopedic Manual Surgical Instruments…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 12, 2016
BLUE IMPERVIOUS GOWN WITH THUMBHOOKS, X-LARGE. Non-Sterile, Single Use Only, Plastic Non-Surgical Isolation Gown…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health
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.