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 Apr 1, 2015
Mini Naan Eight (8) nann packaged in coated paper printed board and transparent wrap with a net weight of 12.6 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.fgf brands, Inc.
FDA (openFDA food enforcement)
Reported Apr 1, 2015
Stonewall Kitchen Buffalo Wing Sauce Net Wt. 17.5 oz. glass jar UPC 711381-31395 4 Item # 251805,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stonewall Kitchen, LLC
FDA (openFDA food enforcement)
Reported Apr 1, 2015
Endo TCS Driver Straight Hexalobe #6 P/N 5210-1004, Non-Sterile, Manufactured by Titan Spine, LLC. Endo TCS driver is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Titan Spine, LLC
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Natural Grocers brand Organic Garlic Powder. Natural Grocers brand Organic Garlic Powder. Packaged in Zip-Lock-type…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vitamin Cottage Natural Food Markets, Inc.
FDA (openFDA food enforcement)
Reported Mar 25, 2015
Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2015
CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2015
TactiSys Quartz Pack, PN-004 400. For percutaneous catheter radiofrequency (RF) ablation of atrial cardiac arrhythmias…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical
FDA (openFDA device enforcement)
Reported Mar 23, 2015
Stock Yards Meat Packing Co., Inc. Retira Producto De Carne Asada (Roast Beef) Debido A Un Posible Error De Rotulacin
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Recalling firm not stated
USDA FSIS
Reported Mar 18, 2015
Arrow Intra-Aortic Balloon Catheter Kit Fiberoptix (IAB), 8 Fr 40 cc Model: IAB-05840-LWS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Mar 18, 2015
GE Healthcare Proteus XR/a with wall stand model number 2260354. Intended for use in generating radiographic images of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Mar 18, 2015
EVOLUTION MP TIBIAL BASE, REF ETPKN8SR, SIZE 8 RIGHT, TYPE PRIMARY, FIT CEMENTED, STYLE KEELED, STERILE R, Rx ONLY,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microport Orthopedics Inc.
FDA (openFDA device enforcement)
Reported Mar 18, 2015
Apollo (cold) Laser Desktop Control Units, Model AP2-DT. The Apollo IR Heat Lamp System is intended to emit energy in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pivotal Health Solutions
FDA (openFDA device enforcement)
Reported Mar 18, 2015
Juno DFR X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Radiology Systems LLC
FDA (openFDA device enforcement)
Reported Mar 18, 2015
Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Mar 14, 2015
Gourmet Kitchen Inc. Recalls Various Beef and Chicken Products Due to Misbranding and an Undeclared Allergen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gourmet Kitchen Inc.
USDA FSIS
Reported Mar 11, 2015
Monaco radiation therapy treatment planning system. The Monaco system is used to make treatment plans for patients with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 11, 2015
DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.iCAD, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2015
Ikaria, INOmax DSIR (Delivery System), Model 10007. Nitric oxide delivery system for use with ventilators.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.INO Therapeutics (dba Ikaria)
FDA (openFDA device enforcement)
Reported Mar 5, 2015
Premier Distribution Center, Inc. Retira Productos De Res Y Cerdo Debido A Un Posible Error De Rotulacin
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Mar 4, 2015
Starburst MRI Semi-Flex Electrode Device, 25cm/Attached Cable/14Ga/6.4F, Product No. H7877001039091, Catalog No.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics
FDA (openFDA device enforcement)
Reported Mar 4, 2015
Set Screw 5.5 mm Rod - Model #7703-1600. Product Usage: The titanium alloy set screw is used to seat a 5.5 mm titanium…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet Spine, LLC
FDA (openFDA device enforcement)
Reported Mar 4, 2015
The Brainlab Offset Cup Impactor Universal. Part of the Brainlab hip system. An intraoperative image-guided…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Mar 4, 2015
The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Mar 4, 2015
HeartWare Ventricular Assist System (HeartWare Controller) Product Usage: For use as a bridge-to-cardiac…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
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.