Recalls distributed in Arizona
These notices name Arizona 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.
3,983 stored notices name Arizona, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Arizona too — those are in the archive.
Reported Jul 9, 2014
BrightView XCT: product code 882482, BrightView X- upgraded with the XCT Flat Panel Detector (FPD): product code…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Physique Enhancing Science ALPHAMINE, Powerful Thermogenic Powder, DIETARY SUPPLEMENT Net Wt. 8.9 oz (252 g). Raspberry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physique Enhancing Science
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 9, 2014
Stryker Orthopaedics Triathlon Tritanium Patella Inserter, . NON-STERILE Product Usage: The Triathlon Tritanium Patella…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Synthes B37 Replacement Screws. M3.5 Screw for insertion handle guide/aiming arm, part numbers 3.113.025 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
MOSAIQ MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. It…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
GSF LLC Shelled Walnuts, Kernel Combo Halves & Pieces, 15% New Wt. 25 lbs. GSF LLC, Visalia, CA 93290
High riskUsing this product could cause serious injury, illness or death — stop using it now.GSF Nut Company LLC
FDA (openFDA food enforcement)
Reported Jul 2, 2014
Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System is intended to provide invasive or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nellcor Puritan Bennett Inc. (dba Covidien LP)
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray System & Brilliance CT Big Bore Radiology Whole…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Ingenia 3.0T R5, magnetic resonance imaging system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Siemens StreamLAB(R) Analytical Workcell; Catalog number 746002.901. Designed to automate sample handling and…
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 Jul 2, 2014
Spacelabs Healthcare Qube Compact Monitor, Model 91390. Intended to alert the user to alarm conditions that are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Western / Scott Fetzer Company
FDA (openFDA device enforcement)
Reported Jul 2, 2014
VerSys¿ Hip System, Beaded Fullcoat Stems, Zimmer, Inc., Warsaw, IN 46581
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jun 25, 2014
Philips/Children's Medical Ventures Smart Monitor 2 Professional Series infant apnea monitor.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Childrens Medical Ventures
FDA (openFDA device enforcement)
Reported Jun 25, 2014
Synergy XVI Intended for radiation therapy treatment.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 25, 2014
Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a component of the Puritan Bennett 840 Ventilator:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nellcor Puritan Bennett Inc. (dba Covidien LP)
FDA (openFDA device enforcement)
Reported Jun 25, 2014
RayStation software version 4.0.3.4 RayStation is a software system designed for treatment planning and analysis of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jun 25, 2014
Spacelabs Healthcare Ventilator Flexport Interface, Model 90436A-07
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Jun 18, 2014
BioDerm Liberty 3.0 External Male Catheter Specialty Type with integral collection chamber (Component: SKIN-PREP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioDerm, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 18, 2014
Cordis EMPIRA RX PTCA Dilatation Catheter Catalog # 85R30300S For cardiovascular use.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jun 18, 2014
Leica Ceiling Mount MSF-1 for use with M841 and M501 operating microscopes. Article Number 10446781 utilizes a supply…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 18, 2014
Horizon Medical Imaging Horizon Medical Imaging is a medical image and information management application that is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported Jun 11, 2014
ExacTrac 5.5, an Image Processing System used for patient positioning for radiation therapy or radiosurgery.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
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.