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.
4,042 stored notices name Arizona, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Arizona too — those are in the archive.
Reported May 29, 2019
Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
75 more products in this recall
FDA (openFDA device enforcement)
Reported May 23, 2019
Blount Fine Foods Recalls Soup with Chicken Products Due to Possible Foreign Matter Contamination
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blount Fine Foods Corp.
USDA FSIS
Reported May 22, 2019
Abbott Alinity ci-series System Control Module software version 2.5.1; LN 3R70-01 with the following hardware: Level…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported May 22, 2019
Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT Estradiol assay is a Chemiluminescent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Compass Health Brands (Corporate Office)
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Frozen ground tuna, 1 lb package, 20 packages/case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jensen Tuna Inc.
FDA (openFDA food enforcement)
Reported May 22, 2019
Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Moller Vital
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Artis Zee (material # 10094135, 10094137, 10094141) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 15, 2019
Neuro Omega System, incorporating HaGuide software. For neurological and neurosurgical use. To monitor, record and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Alpha Omega Engineering
FDA (openFDA device enforcement)
Reported May 15, 2019
Lee's Tea brand of Pink Chai - Organic Spiced Tulsi Tea Blend Loose Leaf Tea packaged in re-sealable plastic pouches…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lee's Provisions Inc.
FDA (openFDA food enforcement)
Reported May 15, 2019
El Guapo Chile Habanero Habanero Chili Pepper 0.5oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCormick & Company, Inc. - Flavor Manufacturing Center
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 15, 2019
Shredded and blocks of Colby & Monterey Jack cheese - Labeled and Packaged: 1) Great Value, Finely Shredded, Colby &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schreiber Foods Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 15, 2019
Atellica IM 1300 Analyzer, Material Number 11066001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 15, 2019
T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Biomet Headless Compression Screws and Twist-Off…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 8, 2019
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), product code 35700BAX - Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported May 8, 2019
FilmArray Gastrointestinal (GI) Panel, IVD, Rx Only, Biofire Diagnostics, LLC REF: RFIT-ASY-0104, and RFIT-ASY-0116),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported May 8, 2019
Losartan Potassium Tablets, USP, 50 mg, 30 tablet bottles, Rx Only, Distributed by: The Kroger Co, Cincinnati, OH…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Legacy Pharmaceutical Packaging LLC
FDA (openFDA drug enforcement)
Reported May 8, 2019
Ethyl Alcohol Enzymatic Assay, (a) REF 0220 (small test kit), (b) REF 0221 (large test kit) Product Usage: Detergent…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lin-Zhi International Inc.
FDA (openFDA device enforcement)
Reported May 8, 2019
EZ Derm Porcine Xenograft, labeled as the following: a. EZ Derm 3x4 (8x10 cm) Non-Perforated, Part Number: 131703-03;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Molnlycke Health Care, Inc.
FDA (openFDA device enforcement)
Reported May 8, 2019
cobas e 801 immunoassay analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported May 1, 2019
St. Jude Medical Confirm Rx Insertable Cardiac Monitor, REF DM3500, Sterile. Product Usage: The St. Jude Medical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott
FDA (openFDA device enforcement)
Reported May 1, 2019
Arthrex Burr, Oval, 12 Flute, 5.5 mm x 13 cm (AR-8550OBT) These devices are indicated for resection of soft and osseous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported May 1, 2019
RT Elements Software revisions of the RT Elements applications have a specific software version number. Specifically…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported May 1, 2019
OnSight 3D Extremity System- X-Ray, Tomography Computed System Catalog Numbers: 1743566 (w/ Attached Console) 1743574…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, 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.