All recall categories

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.

Food

Reported Mar 8, 2017

Pepper Jack Cheese Half Moons, 15pkgs/case UPC 78279600895

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Papa John's Salads & Produce, Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 8, 2017

Deep River Sour Cream & Onion Krinkle Kettle Chips 2 oz bag UPC 8 50668 00049 8 & 5 oz bag UPC 8 50668 00099 3

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Shearers Foods, LLC

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 8, 2017

Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Windstone Medical Packaging, Inc.

123 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 1, 2017

AMT Bridle - Nasal Tube Retaining System Used with Nasogastric/Nasointestinal (NG/NI) tubes.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Applied Medical Technology Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 1, 2017

Trader Joe's Harvest Whole Wheat Bread; NET WT 24 oz. (1 lb. 8 oz.) SKU 00132; UPC: 0000 1328. Distributed and sold…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Athens Baking Company

FDA (openFDA food enforcement)

Medical devices

Reported Mar 1, 2017

ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 ETEST is a quantitative technique for determining the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioMerieux SA

FDA (openFDA device enforcement)

Food

Reported Mar 1, 2017

A) Palmer's Candies Chocolate Almond Bark , NET WT 9 OZ (255 g) packaged in plastic clamshell container, UPC…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Palmer and Company, dba Palmer Candy Co.

17 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 1, 2017

Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tosoh Bioscience, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 1, 2017

GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The GrebSet micro-introducer…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Vascular Solutions, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 22, 2017

Burts British Hand Cooked Potato Chips Sea Salt & Malted Vinegar 150gx10 and 40gx20

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bwi Inc.

FDA (openFDA food enforcement)

Meat & poultry

Reported Feb 22, 2017Updated Oct 23, 2026

Fratelli Beretta USA, Inc. Recalls Mortadella Product Due To Misbranding and Undeclared Allergens

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Fratelli Beretta USA, Inc.

USDA FSIS

Medical devices

Reported Feb 22, 2017

Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The handle is used to hold surgical components…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 22, 2017

BrightView XCT

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 22, 2017

LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 22, 2017

CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network…

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)

Medical devices

Reported Feb 15, 2017

Celerity ECG Cable Accessory Pack, STERILE, Rx ONLY - distributed under the following labels: (a) angiodynamics…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Angiodynamics Inc. (Navilyst Medical Inc.)

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A single PRO2 device is packaged in a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

AtriCure, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teleflex Medical

FDA (openFDA device enforcement)

Food

Reported Feb 15, 2017

DANONE¿ DAIRY DRINK NUT AND CEREAL 7.7 FL OZ (229mL) bottles, UPC 36632 01421

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Dannon Company, Inc.

FDA (openFDA food enforcement)

Drugs

Reported Feb 15, 2017

Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

VistaPharm, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Feb 8, 2017

Olympus Scientific Solutions Americas Corporation (OSSA) VANTA¿ XRF Analyzer. Model Vanta VCR and Vanta VMR…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympus Scientific Solutions Americas

FDA (openFDA device enforcement)

Food

Reported Feb 8, 2017

Jon Donaire Ice Cream Layer Cake, Deliciously moist white cake with rich, creamy strawberries & cream ice cream, NET WT…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Rich Products Corp.

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 1, 2017

FRONT: Stauffer's Animal Crackers Original; Net Wt. 32 OZ.; BACK: (best by date): 07SEP17; (bag lot numbers) LC120716…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

D. F. Stauffer Biscuit Co., Inc.

FDA (openFDA food 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.