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.

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.

Medical devices

Reported Dec 26, 2012

Invacare Height Adjustable (walking) Canes, Model Numbers: 8916, 8917, and 40918-6. The device is packaged six (6)…

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

Invacare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 26, 2012

ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mobility impaired person in a…

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

ThyssenKrupp Access Corp.

FDA (openFDA device enforcement)

Food

Reported Dec 19, 2012

Berres Brothers Coffee Roasters Chocolate & Peanut Butter regular whole bean coffee packaged in the following sizes: 12…

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

Berres Brothers, Inc.

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 19, 2012

Baby Quasar (LAB-001-D, BQ101) and Baby Quasar Pink (LAB-046-A BQ101-P) are infrared LED lamps that are labeled in…

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

Quasar Bio-Tech, Inc. dba Silver Bay LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 19, 2012

Cobas b 123 POC system cobas b 123 POC system is fully automated POC system for whole blood in vitro measurement of pH,…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 19, 2012

The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-resolution color camera, an…

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

Verathon, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 12, 2012

Organic Gelato Chocolate Peanut Butter, 5 liter, contained in plastic packaging, manufactured by Fresca Foods, CO.

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

Boulder Ice Cream

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 12, 2012

Sara Lee Butter Streusel Coffee Cake, Net Wt. 11.5 oz ; 8 cakes per 5.75 lb case; Distributed by Sara Lee Corp.,…

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

Hillshire Brands Company

FDA (openFDA food enforcement)

Medical devices

Reported Dec 12, 2012

Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is intended…

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 12, 2012

The product has the Catalogue/Part number 60010. Olympic Cool-Cap System is a selective head cooling system for…

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

Natus Medical Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Dec 12, 2012

OmniGuide BP-ROBOTIC ( BeamPath Robotic), Single Use Cat. # BP-ROBOTIC The OmniGuide Fiber is indicated for the…

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

OmniGuide, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 12, 2012

Ground limestone also known as calcium carbonate. Omya's food grade ground limestone products. All bulk with no product…

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

Omya Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 12, 2012

Cobas 8000 Modular Analyzer Series, Model/Catalog/Part Number: 05641489001. The Cobas 8000 is a fully automated system…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 12, 2012

Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method is an in vitro diagnostic test for the…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 5, 2012

Echo Bi-Metric Press-Fit Stems/Echo Bi-Metric 11mm x 135mm Collarless Porous Stem (Orthopedic Implant) Indications: 1)…

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

Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 5, 2012

IO FiX X-Post Reamer, Extremity Medical, www.extremitymedical.com; Customer Service: 888.499.0079 The X-Post Reamer is…

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

Extremity Medical LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 5, 2012

The brand name is MRidium Series 1000 MR Infusion Sets, Type 1058 MR IV Extension Set, Lot Code LBG001. The generic…

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

Iradimed Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 5, 2012

Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated…

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

Kimberly-Clark Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 5, 2012

Kroger Deluxe French Vanilla Magnifique Ice Cream, 48 FL OZ laminated carton. INGREDIENTS: MILK, CREAM,…

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

Kroger Co.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 5, 2012

100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…

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

Terumo Cardiovascular Systems Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 5, 2012

Chicken of the Sea Solid White Tuna in Water, 7 oz., 48 cans per case (case: 6 sets of multi-unit packs of 8 cans…

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

Tri-Union Seafoods, L.L.C dba Chicken of the Sea.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 5, 2012

NexGen CompleteKnee Solution Stemmed Nonaugmentable Tibial component The NexGen¿¿ system is a semiconstrained,…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

bioMerieux BacT/ALERT Control Module, catalog number 210147, Clinical instrument The product is most commonly used to…

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

Biomerieux Inc.

31 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

IO Fix IntraOsseous Fixation System; Extremity Medical. www.extremitymedical.com; Customer Service: 888.499.0079. The…

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

Extremity Medical LLC

FDA (openFDA device enforcement)

Free recall alerts

Get alerted about new Arizona recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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.