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.
Reported Jul 11, 2018
microTargeting" Drive System, Product Number MT-DS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FHC, Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 6, 2018
Tillamook Country Smoker, LLC Retira Productos De Carne Seca (Jerky) De Res Listos Para Consumir Debido A Un Error De…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tillamook Country Smoker, LLC
USDA FSIS
Reported Jul 4, 2018
Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle Supplement Facts Serving Size:***Vitamin B-12 (as…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Absonutrix
FDA (openFDA food enforcement)
Reported Jul 4, 2018
HLD Systems 600 Series Washer/Pasteurizer, UDI (01) 0085249007009 (11) 160929 (21) 61160; Model 610HT, 115V & Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cenorin, LLC
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intersurgical Inc.
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Single Chamber Temporary External Pacemaker, Model 53401
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Jul 4, 2018
RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jul 4, 2018
ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model 10849000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2018
Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
VNS Therapy Programmer, Model 3000, v1.0 System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Fabius GS Premium Anesthesia Machine; Cat. no. 8607000 Product Usage: Inhalation anesthesia machines for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 27, 2018
Kellogg's Honey Smacks, 15.3 oz. and 23 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kellogg Company
FDA (openFDA food enforcement)
Reported Jun 27, 2018
Nitinol Staple, Elastic Staple Large-Asymmetrical, Sterile R, Model #: a) ES-18x15x17; b) ES-18x17x19
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TriMed Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Biomet Modular Primary Tibial Tray Implants; Modular Interlok Primary Tray (size 75 mm); Item No. 141215; UDI: (01)…
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 Jun 13, 2018
Alaris Extension Sets with microbore tubing Model 20022 and 30914 Is used to administer fluid and medications from a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Draeger Jaundice Meter JM-103 The device is intended for use in hospitals, clinics or doctor s offices under a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity PACS-IW with Universal Viewer is a device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 13, 2018
Heritage Shortbreaad Lemon Infused Ingredients: Enriched flour, pasteurized cream(milk),sugar, salt, pure crystallized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heritage Short Bread, Inc.
FDA (openFDA food enforcement)
Reported Jun 13, 2018
Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, Multiple sizes: 8 oz, 16 oz, 32 oz, 64 oz, 1 gal, 2.5 gals, 5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lake Michigan Distilling Co. LLC
FDA (openFDA food enforcement)
Reported Jun 13, 2018
Restoris MCK Onlay Insert Extractor.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Jun 6, 2018
Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators, Catalog No C650-129A (00821925008700) The cord consists…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gyrus Acmi, Incorporated
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.