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.
4,043 stored notices name Arizona, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach Arizona too — those are in the archive.
Reported Mar 9, 2016
Apple Caramel Almond Tea, Bag Size - 2lbs Minimum, Bulk Packaging, Item No. FB-004
High riskUsing this product could cause serious injury, illness or death — stop using it now.International Tea Importers
FDA (openFDA food enforcement)
Reported Mar 9, 2016
Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for single or multi-compartmental knee…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Mar 9, 2016
Maquet Getinge Group 1180.19XO Extension Device. Manufacturer MAQUET GmbH, Used to support the upper and lower…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular US Sales, LLC
FDA (openFDA device enforcement)
Reported Mar 9, 2016
Medtronic Custom Perfusion Tubing Pack, Rx, Sterile EO. Terumo Cardiovascular Systems (Terumo CVS) has distributed an…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Mar 9, 2016
BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2016
(Stryker) AccuPlace Straight Level Needle Guide; Assists the user with inserting a needle at a predetermined angle for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 3, 2016
Namias Of Arizona Retira Productos De Pollo Por Un Error De Rotulacin Y Alrgenos No Declarados
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carlotta's Kitchen LLC
USDA FSIS
Reported Mar 2, 2016
HipLOC CHS Plate/Lag Screw Introducer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2016
EkoSonic Endovascular System, Catalog Number 500-56112. It consists of three main components, a single use EkoSonic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.EKOS Corporation
FDA (openFDA device enforcement)
Reported Mar 2, 2016
Hill-Rom Bariatric Power Recliner, Product Model # P9096 Hill-Roms 660 lb Powered Bariatric Recliner was created to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2016
This reagent is for in vitro diagnostic use. Pax-5 (1EW) monoclonal antibody is intended to be used for the qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2016
software for Syngo Dynamics a Picture Archiving and Communication System (PACS) intended for acceptance, transfer,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2016
Synthes Small Electric Drive (SED)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Feb 24, 2016
REF 0038460 Toomey Syringe 70cc Syringe with Catheter Tip and Luer Tip Adapters, Single Use, Rx Only, Latex Free, 50…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Feb 24, 2016
CEA / CD66e Ab-2, Product code RB-368-R7, RB-368-R1; 7 ml each. Description Carcinoembryonic antigen (CEA), is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lab Vision Corporation
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Arctic Sun 5000 and Arctic Sun 2000; Intended for monitoring and controlling patient temperatures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2016
RadSuite, a picture archive and communications system. Model Numbers Versions 5.30.0, 5.30.1, 5.30.2, 5.30.2 SB0344,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2016
IMPLANT,TM, MTX 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMM4B10 Product Usage: Zimmer Dental implant systems are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Dental Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Zzang! Original Candy Bar, 2.5 oz., packaged in preprinted cardboard boxes, UPC 8 44397 00014 0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zingerman's Candy Manufactory
4 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 10, 2016
Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080. Volume controlled emergency and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 10, 2016
The ABX PENTRA Cholesterol CP ref. A11A01634 is an in vitro diagnostic assay for quantitative determination of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Horiba Instruments Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 10, 2016
Tong Ren Tang Shenjing Shuairuo Wan Herbal Supplement 240 pills UPC Code: 6 904579 129602 Distributed by: Solstice…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Madison One Acme Inc.
FDA (openFDA food enforcement)
Reported Feb 10, 2016
Dove Chocolate Assortment Snowflakes Net. Wt. 24.0 oz. Distributed by Mars Chocolate na, llc Hackettstown, NJ…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mars Chocolate North America
FDA (openFDA food enforcement)
Reported Feb 10, 2016
Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-invasive homecare devices, for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Resmed Corporation
FDA (openFDA device enforcement)
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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.