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 48,100 notices were distributed nationwide, so they reach Utah too — those are in the archive.
Reported Aug 22, 2018
Rio System Irrigation Clip - Catalog # 111690 Product Usage: The RESTORIS Partial Knee Application (PKA) for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Aug 22, 2018
1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Boston Scientific Guider Softip XF Guide Catheter Product Usage: Is a neurovascular access catheter that creates a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Aug 15, 2018
JouJou's white large pita bread
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Constantine's International Foods
FDA (openFDA food enforcement)
Reported Aug 15, 2018
119" Blood Set w/200 Micron Filter, Clave¿, Rotating Luer, Sterile The blood tubing accessory with CLAVE Connector is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
52 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For PTZ Video Ext, IP PTZ HD ErgoJust Video…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Seattle Sourdough Pub Buns 6 pack, net wt. 16 oz., UPC 0-72220-10164-5
High riskUsing this product could cause serious injury, illness or death — stop using it now.Portland French Bakery L T D
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 15, 2018
Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Aug 15, 2018
utz Carolina Style Barbeque Potato Chips, Net Wt 2.875 OZ, UTZ Quality Foods, LLV, Hanover, PA 17301, UPC:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Utz Quality Food Inc.
FDA (openFDA food enforcement)
Reported Aug 15, 2018
Waterpik Sonic-Fusion Professional, Model: SF-02 Product Usage: The device is composed of a unit base and an oral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Water Pik, Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-9300;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cayenne Medical Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Instrument trays used to store AltiVate Small Shell Trials (FA S ALTIVATE RSP HUM TRLS SM). Metal container with lid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Aug 8, 2018
1) ELITE HV, Hemostasis Valve Introducer System, Sterile EO, Rx Only, Catalog #: a) BCL-100-04; b) BCL-100-05; c)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galt Medical Corporation
7 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2018
MAYFIELD INFINITY XR2 BASE UNIT, Part Number A2079 The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2018
XLTEK EMU40EX EEG Headbox
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Homestyle Seasoned Croutons: 4 oz. foil pouch Item # 73689 UPC 10083661736898 Sugar Foods Corporation 6190 E. Slauson…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sugar Foods Corporation Inc.
9 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 1, 2018
AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N utilizing raw material (RM0677) from the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ad-Tech Medical Instrument Corporation
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulating…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Medical Division
FDA (openFDA device enforcement)
Reported Aug 1, 2018
CORAIL Cementless Femoral Stem HA Coated Standard Size 11, Catalog No. 3L92511
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2018
MR Surgical Suite Option Product The MR Surgical Option when integrated with the GE Signa¿ 3.0T or 1.5T magnetic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
FDA (openFDA device enforcement)
Reported Aug 1, 2018
ImplantDirect, Dental implants intended for use in partially and fully edentulous upper and lower jaws in support of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Gibco CTS OpTmizer T Cell Expansion Serum Free Medium, bag format, Model Numbers A1048503 and A1022103. Tissue and cell…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies, Corp.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Superfood Salad Kit - 6.8 lbs. - sold to Kroger owned stores and prepared and purchased at deli department at retail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Papa John's Salads & Produce, Inc.
FDA (openFDA food 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.