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 Jul 3, 2013

Quick Connect QLC1677E, QRC1699E, QPC1721E and QFC1683E. STERIS Corporation, Mentor, OH 44060 QLC1677E, QRC1699E,…

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

Steris Corporation

FDA (openFDA device enforcement)

Food

Reported Jun 26, 2013

Lightlife Farmer's Market Veggie Burgers, meat free, 12 oz/4-count bag, packaged in 5/12 oz-bag/cartons. Distributed…

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

Conagra Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 26, 2013

Echelon, Echelon Oval and Oasis MR imaging device systems; one unit per box. The Echelon, Echelon Oval and Oasis MR…

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

Hitachi Medical Systems America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2013

VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog# 6802002. Used to quantitatively measure total…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2013

GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 reusable blades Product Usage: The…

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2013

Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame adapter assembly is intended to be used by qualified…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 19, 2013

Market Pantry, Sweet & Salty Mix, NET WT 3 oz (85g), UPC 0 85239 08131 0, INGREDIENTS: Peanuts (peanuts...) ...Honey…

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

American Importing Co., Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 19, 2013

TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1 Tissue Removal System is indicated for use in…

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

American Optisurgical Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 19, 2013

XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and…

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

Atlantic Pro Nutrients, Inc. dba XYMOGEN

FDA (openFDA food enforcement)

Medical devices

Reported Jun 19, 2013

embla Embletta Gold (It functions as a Polysomnography Recorder and Ventilator Effort Recorder). The Embletta Gold is a…

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

Embla System LLC

FDA (openFDA device enforcement)

Food

Reported Jun 19, 2013

"Shurfine CREAMERY SELECT PREMIUM ICE CREAM Dulce de Leche Caramel Swirled in Caramel Ice Cream KEEP FROZEN 1.75 QUARTS…

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

Southwest Ice Cream Specialties

FDA (openFDA food enforcement)

Medical devices

Reported Jun 12, 2013

FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray.

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

American Optisurgical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT Biliary SES product is indicated for…

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

Cordis Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

Canister: CO2 canister with GE part numbers 1407-3200-000, 1407-7004-000, or M1084850. Intended to provide general…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Jun 12, 2013

Cottage Cheese with Chive distributed under the following labels and sizes: (a) Hood brand Cottage Cheese with Chive,…

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

HP Hood LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 12, 2013

LPC Fine Mesh Cassette for the Leica LPC Printer. Part No: 14060546848; 14060546846; 14060546845; 14060546933;…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G, # 3100Y, # 3100W; Product is…

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

Maytex Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

REF 8229705 x1 NIM TriVantage EMG Endotracheal Tube 5.0 mm I.D. x 6.5 mm O.D. Medtronic Xomed, Inc., 6743 Southpoint…

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

Medtronic Xomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2013

AngioDynamics Micro Introducer Kits under the following labeling: 1) AngioDynamics 4F Standard Micro-Introducer Kit,…

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

Angiodynamics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2013

EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.

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

Nephron Pharmaceuticals Corp.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2013

Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Plunger Delivery System, 4", Part…

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

Orthovita, Inc., dba Stryker Orthobiologics.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2013

***REF S-3D*** 3mm Diamond Ball. Used for cutting and shaping bone.

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

The Anspach Effort, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a…

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

Alere San Diego, 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.