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 Jul 29, 2015
0702-001-350Q, Diverter Valve Assembly 0702-001-000, Neptune 2 Rover Ultra (120V) 0702-001-000R, Repair Neptune 2 Rover…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Various OxyTOTE Portable Oxygen System regulators, Valve Integrated Pressure Regulator, one unit per package. Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Western / Scott Fetzer Company
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Musculoskeletal Transplant Foundation, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1: The Nidek Green Laser Photocoagulator…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Apex ARC Hip Stem, HA Coated, Size 5; Product Code: HC-21005-HA Product Usage: The Apex ARC Hip Stem is the femoral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Omnilife Science Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2015
16mm Chisel Blade; used in the LCP Anterior Ankle Arthodesis Plate System and the Hip Preservation Surgery Set.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Natural Grocers Caribbean Fruit & Nut Mix, Net Wt. (10 oz) (283g), packaged in plastic bag.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vitamin Cottage Natural Food Markets, Inc.
FDA (openFDA food enforcement)
Reported Jul 15, 2015
Spicy Black Bean Burger powder mix, packaged in 30 LB poly-lined Kraft bags.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coalescence LLC
FDA (openFDA food enforcement)
Reported Jul 15, 2015
Breast Pack - contains Devon Light Glove Used during surgery
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stradis Healthcare, LLC.
50 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Jul 8, 2015
HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac transplantation in patient who are at risk of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Medtronic DLP Femoral Arterial Cannula, models 57414, 57417, and 57421, and DLP Femoral Cannula Replacement Kit, Models…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Infinite F500, in vitro diagnostic. Product Usage: The Tecan Infinite F500 is a multifunctional microplate reader with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Natural Knee II Revision Femoral Stem, 125mm, item 6215-12-185. packaged in configuration 803/791. Knee Prosthesis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2015
Lombardi Brothers Meats Recalls Steak and Ground Beef Products Due To Possible E. Coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lombardi Brothers Meats
USDA FSIS
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)
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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.