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 48,100 notices were distributed nationwide, so they reach Arizona too — those are in the archive.
Reported Dec 16, 2020
HomeChef Meal kit:One-Sheet Pretzel-Crusted Chicken with roasted broccoli and honey mustard..31.0 OZ (1 LB 15 OZ) 879g
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Kroger Co.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 16, 2020
ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Welch Allyn, Inc/mortara
FDA (openFDA device enforcement)
Reported Dec 9, 2020
CME America T-Syringe Pump -T34L - Product Usage: infusion of medications or fluids requiring continuous or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CME America, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 9, 2020
Dole" Organic Romaine Hearts 3pk Organic Biologique) (UPC 0-71430-90061-1), Wild Harvest Organic Romaine Hearts, Net Wt…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Dec 9, 2020
YAGUMO AMANATTO GIFT BOX 6P 6/19.01 OZ JAN Code: 49 03089 39050 4 Imported by JFC International Inc. Los Angeles, CA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J F C International Inc.
FDA (openFDA food enforcement)
Reported Dec 9, 2020
BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coloplast Manufacturing US, LLC
FDA (openFDA device enforcement)
Reported Dec 2, 2020
EMPOWR Partial Knee Peg Drill Guide; Model: 800-06-007.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom Manufacturing, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Sysco Arrezzio 3/8" Petite Diced Tomatoes in Tomato Puree, #7807458, each metal can has the net weight of 6.38 lbs.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Neil Jones Food Company
FDA (openFDA food enforcement)
Reported Dec 2, 2020
Natural Grocers, Elderberries Whole Organic, 4 oz. (113g), plastic bag, UPC 0-0082-00304-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vitamin Cottage Natural Foods Market, Inc. dba Natural Grocers
FDA (openFDA food enforcement)
Reported Nov 25, 2020
Art Of Tea - Feel Better tea; Produced and Distributed by: Art of Tea LLC, Monterey Park, CA Directions: 1 Tbsp of tea…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Art Of Tea
FDA (openFDA food enforcement)
Reported Nov 25, 2020
Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 25, 2020
VNS Therapy¿ AspireSR¿ Generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2020
COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Elastic Traction Device, 11mm Lower. UPN: ER56041 Reference Number: ETD-D-26-235-C-N - Product Usage: indicated for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro-Tech USA
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thomas Scientific
FDA (openFDA device enforcement)
Reported Nov 18, 2020
SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Product Usage: intended for use in the dermatologic and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesthetics Biomedical, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Strep B Carrot Broth One-Step, Ref. Z40, UDI: 00819398026499
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Blood Monitoring Unit (BMU 40), model no. 701040852 - Product Usage: is to monitor blood parameters during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular US Sales, LLC
FDA (openFDA device enforcement)
Reported Nov 18, 2020
QUIDEL Sofia SARS Antigen FIA IVD REF 20374
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Niobe ES System, Models 001-006000-1 and 001-006100-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stereotaxis Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2020
XTANT Medical, ## mm x ## mm x # mm x # ,Lordotic/Packaged InTice - C, Sterile R, Single Use Only, for the following…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.XTANT Medical
FDA (openFDA device enforcement)
Reported Nov 11, 2020
Fixed Core Wire Guide, RPN TSCF-35-260-3, GPN G00517. The product is a curved wire guide with PTFE coating manufactured…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook 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.