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 Dec 30, 2015
A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization and fixation of fractures, revision…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Optional PS500 Power Supply Unit for the Evita V500 Ventilator and Babylog VN500 Ventilator. Babylog VN500 is a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 30, 2015
FB Broth, 10ml (Fastidious Bacteria Broth) Cat. no: K31 Lot: 15231 A fastidious bacteria broth for the enriched…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Hook Blade, Angled. Part number 7058A. Sterile disposable blade for use with Endoscopic Tarsal Tunnel Decompression…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instratek, Incorporated
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Double Trigger Handpiece. Rx only Made in Switzerland
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 23, 2015
MYLA CLINIC PATCH 3.2.0 CD Product Usage: MYLA is a computer application ( Middleware ) based on Web 2.0 technology…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 23, 2015
MOSAIQ Oncology Information System. Used to manage workflows for treatment planning and delivery.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Dec 23, 2015
Unolok Blunt Fill Needle 18G x 1.5" Red, Sterile, Single use, Non-injectable needle, Single use, non-injection needle
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Myco Medical Supplies Inc.
FDA (openFDA device enforcement)
Reported Dec 16, 2015
GE Healthcare, Revolution CT Scanners. Revolution CT- The system is intended for head, whole body, cardiac and vascular…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
FDA (openFDA device enforcement)
Reported Dec 16, 2015
Kroger 100% natural apple FROM CONCENTRATE 64FL OZ. INGREDIENTS: APPLE JUICE FROM CONCENTRATE (FILTERED WATER, APPLE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Kroger Co.
FDA (openFDA food enforcement)
Reported Dec 16, 2015
Organic blenditup Protein + Plant Based Smoothie Mix, No Dairy, Vitamin Fortified, 100% Vegan, Mild Natural Flavor with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thrive Foods LLC
FDA (openFDA food enforcement)
Reported Dec 16, 2015
Valeant Pharmaceuticals North America Model No. Spag-2 Small Particle Size Aerosol Generator SPAG-2 6000 is a pneumatic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Valeant Pharmaceuticals North America LLC
FDA (openFDA device enforcement)
Reported Dec 9, 2015
Kozy Shack Indulgent Salted Caramel
High riskUsing this product could cause serious injury, illness or death — stop using it now.Land O' Lakes, Inc.
FDA (openFDA food enforcement)
Reported Dec 9, 2015
Radiesse (+) Lidocaine Injectable Implant 1.5cc, P/N: 8063M0K1. Indicated for subdermal implantation for the correction…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 9, 2015
Prostin Injection 10 mcg/mL, 25 mcg/mL, 50 mcg/mL, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Western Drug
90 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 2, 2015
Dimension Vista System (MG) ; Flex reagent cartridge Catalog number K3057, SMN 10445158. For the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 25, 2015
Cyberonics Vagus Nerve Stimulator (VNS) Therapy AspireSR Generator, Model 106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2015
Cucumber, Super Select Unspecified variety packed in Hello Fresh box the week of August 24-28-2015 in the meal Spicy…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Grocery Delivery E-Services USA, Inc.
FDA (openFDA food enforcement)
Reported Nov 25, 2015
Kar's Sweet n' Salty Mix Box of 18, 3.5 oz. flexible film bags. 1 box per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kar Nut Products Company
10 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 25, 2015
GMK Hinge knee prosthesis; Model Number: 02.09.TA410; Orthopedics and Orthopedic Surgery
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medacta USA
FDA (openFDA device enforcement)
Reported Nov 25, 2015
Synthes Application Instrument for Sternal ZIPFIX. Indications for use include primary or secondary closure/repair of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Nov 18, 2015
5/4 Limited Edition Cucumber Carton, Sizes 24SP, 36/36SP, 48. These cucumbers are shipped in a black, green, yellow,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Andrew & Williamson Fresh Produce
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 18, 2015
Smooth Muscle Action (SMA) Immunohistochemistry reagent. Catalog numbers: CME305A-0.1ml; CME305B - 0.5 ml, PME305AA -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biocare Medical, LLC
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Biomet 3i Narrow Right Angle Large Driver Tip (Hexed). Driver tips are attached to a surgical drilling unit to carry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
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.