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 1, 2015
LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2015
SNOBIZ CHEESECAKE SHAVE ICE FLAVOR, 10 pouches/carton; 8 cartons/case (80 pouches total per case), 104 gram per pouch,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Crystal Fresh
FDA (openFDA food enforcement)
Reported Jul 1, 2015
Epi breads, 7" French Hoagie Sliced, Net Weight 10.4 lbs., Lavoi Corporation, EPI Breads, 4710 West Ledbetter, Dallas,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lavoi Corporation d/b/a/ Epi De France
21 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 1, 2015
Merit Medical Prelude Pro Sheath Introducter, 6F (2.0mm) 11cm, REF PRO-6F-11-038, Sterile EO The Merit Prelude Sheath…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2015
Amerigel Hydrogel Gauze Dressing 2 x 2, A5002. Wound Management.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
FDA (openFDA device enforcement)
Reported Jun 24, 2015
HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100,1101,1102,1104,1104JP and 1205.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2015
ELI 380 Electrocardiograph. The ELI 380 is intended to be a high-performance, multichannel resting electrocardiograph.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mortara Instrument, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2015
CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
BBL Port A Cul tubes, catalog number 221606. Patient sample collection tubes. BBL Port A Cul tubes, jars and vials…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage: Inhaler therapy that converts liquid medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Compass Health Brands
FDA (openFDA device enforcement)
Reported Jun 17, 2015
GE OEC Brivo 865 plus, Mobile X-ray system laser aimer assemblies (part number 520002DW)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100, 1101,1102,1104,1104JP and 1205.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Rugby Poly Vitamin Liquid, 50ml
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharmatech LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 17, 2015
Low Volume Extension Set, 72' w/Clamp FLL/MLL APV=1.3ml, STERILE, AND FLUID PATH NONPYROGENIC UNLESS PACKAGE IS DAMAGED…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical Asd Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
M/L Taper with Kinectiv¿ Technology. prosthesis, hip, semi-constrained (metal uncemented acetabular component) Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2015
Oncentra Brachy radiation therapy planning software designed to analyze and plan radiation treatments in three…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2015
Oregano, Mediterranean ground, stock code 03355, packaged in 0.2 lb., .75 lb., 0.8 lb., 1 lb., 4 lbs., 10 lbs., 15…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Regency Group, Inc., The
10 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 3, 2015
EliteCore Full Core Biopsy Device. EliteCore 18G, 20cm with and without HiLiter tip, 15 cm with and without HiLiter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jun 3, 2015
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 27, 2015
ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip, Product Usage: The instruments have application in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported May 27, 2015
Smith's Bakery brand fresh carrot cake, net weight 5 ounces 7 50903 91714 0, 22 ounce 1.38 pound 1/8 Sheet) 7 70118…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Smith's Food And Drug, Inc.
FDA (openFDA food enforcement)
Reported May 20, 2015
Nuclear Gamma Cameras (ADAC Vertex Classic, ADAC VERTEX PLUS/SOLUS/CARDIO, ADAC VERTEX V60) Philips Medical Systems,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 20, 2015
Poco Dolce Bittersweet Chocolate: Burnt Caramel Tile, sea salt topped; 0.6 oz (17 grams) San Francisco CA. Ingredients:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Poco Dolce Confections, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported May 20, 2015
Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component of the Mercury Spinal System, comprised of a variety of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Spinal Elements, Inc.
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.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.