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 Jan 22, 2020
ADVANCED ENDOSEE System CANNULA, Cooper Surgical Product Code/Model Number: ESPX5 The Advanced Endosee Cannula…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2020
QuickDraw Venous Cannula, REF: QD22, UDI: 00690103182699; and REF: QD25, UDI: 00690103182705
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Jan 22, 2020
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2020
ImplantDirect InterActive Precision IO Scan Adapter, Part #6534-09PT, Platform: 3.4mm, Non-Sterile, Rx. The firm name…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2020
Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries, Inc. 306
FDA (openFDA device enforcement)
Reported Jan 15, 2020
Cios Alpha, Model Number 10308191; mobile X-Ray system designed to provide X-ray imaging of the anatomical structures…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2020
GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TFI Holding dba Grey Ghost Bakery
FDA (openFDA food enforcement)
Reported Jan 8, 2020
i-STAT cTnI cartridge
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Point Of Care Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
Chicken of the Sea Sardines in Water; Net Wt. 3.75 oz. (106g) UPC 0 48000 00707 0 18 Individual items per case…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Chicken of the Sea
FDA (openFDA food enforcement)
Reported Jan 8, 2020
PCA Skin Blemish Control Bar, 3.2 oz/90g, Salicylic acid 2% - Acne cleanser, For external use only, Distributed by PCA…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Island Kinetics, Inc. d.b.a. CoValence Laboratories
FDA (openFDA drug enforcement)
Reported Jan 8, 2020
Invia Foam Dressing Kit with FitPad - X-Large (3 pcs) SKU # 0876224. The Invia Foam Dressing Kit with FitPad consists…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medela Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
Medicrea Pass LP, REF B02217545, Non Sterile, Material: Ti-6Al-4V ELI, VIS PEDICULAIRE POLYAXIALE 7.5MM x 45MM,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medicrea International
FDA (openFDA device enforcement)
Reported Jan 8, 2020
NIDEK Specular Microscope, Model CEM-530 - Product Usage: The device provides noncontact, high magnification image…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Nidek, Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
Juno DRF, Model Number 709020 - Product Usage: General. multi-function x-ray systems capable of routine radiographs and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Sistemi Medicali S.P.A.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
STA UNICALIBRATOR (ref. 00675)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
R.H. Macys & Co. Roasted Salted Cherries Berries and Nuts with Dark Chocolate, in 10oz metal tin, UPC - 788709600362
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferris Coffee and Nut Company, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2020
VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy
High riskUsing this product could cause serious injury, illness or death — stop using it now.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mazor Robotics Ltd.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Allergan PLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Alliance Tech Medical, Inc. All Flow Pulmonary Function Filters, 100 filters individually packaged in a clear, sealed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alliance Tech Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 25, 2019
QuickTox 5 Panel Drug Screen DipCard
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ameditech Inc.
FDA (openFDA device enforcement)
Reported Dec 25, 2019
OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT, Catalog Number: ORB-60F - Product Usage: pre-calibrated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
4 more products 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.