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 Mar 5, 2014

The FOCUS is a microprocessor controlled intra-oral x-ray unit with a Load Matching Frequency (LMF) DC generator, which…

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

Instrumentarium Dental, PaloDEx Group Oy

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

VITROS Chemistry Products Na+ Slides, manufactured by Ortho Clinical Diagnostics 513 Technology Blvd Rochester, NY…

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

Ortho-Clinical Diagnostics

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

Single and Dual use Emission Computer Tomography gamma cameras (BrightView XCT, BrightView X & BrightView SPECT)…

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 Mar 5, 2014

HeartStart MRx Monitor/Defibrillator; Model(s), Catalogue, or Code Number: M3535A, M3536A, M3536J, M3536MC The…

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

Philips Medical Systems, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

pCO2 D788 Membranes. Distributed by Radiometer America, Inc., Westlake, OH. An automatic or semi-automatic instrument…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

Renasys EZ, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy System

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

Smith & Nephew Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 5, 2014

Ginger Snap Cookies, 12 oz., Item Code: 48918, UPC 0-41380-23359

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

Unified Grocers Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 5, 2014

PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully upholstered,…

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

Winco Mfg., LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2014

Aesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Adjustment shunt system is intended to shut…

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

Aesculap, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 26, 2014

Canadian Firm Recalls Various Meat Products Without Import Inspection

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

Canadian Firm

USDA FSIS

Medical devices

Reported Feb 26, 2014

Synergy XVI XVI can incorrectly calculate the target position of the treatment table, because of an error that does not…

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

Elekta, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2014

GE Healthcare, PET Discovery 610, Discovery 710, Discovery 600 and Discovery 690. The GE Discovery XR and XA Systems…

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2014

Gelzone Shoulder Sleeve, Catalog Number SLV634, Lot Number 852766. Product Usage: To be used where limb support and/or…

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

Implantech Associates Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2014

Merit Medical's Custom Procedural Trays or Kits containing 1% Lidocaine HCl Injection, USP, 10 mg/mL, Lot 25-090-DK.…

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

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 26, 2014

Digestive enzyme capsules sold under the NOW Foods, Beeyoutiful, Best in Nature, Bluegrass Naturals Vitamin Company,…

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

NOW Foods

FDA (openFDA food enforcement)

Food

Reported Feb 26, 2014

STEMALIVE, 90 Capsules. The product is in a white plastic bottle with white lid, the brand is StemVida International…

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

Stemvida International Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2014

Malibu Polyaxial Screwdriver, 8.0 Plus, Model Number 91-2109; Malibu Polyaxial Screwdriver, Standard, Model Number…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2014

enGen Track System with enGen Select v5.0 with autoverification enabled Product The VITROS 5,1 FS Chemistry System with…

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

Ortho-Clinical Diagnostics

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2014

XiO RTP System. Used to create treatment plans for any cancer patient for whom external beam radiation therapy or…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2014

Diagnostic imaging systems (GEMINI LXL Model #882412, TruFlight Select Model #882438, GEMINI TF PET/CT16 Model #882470,…

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 Feb 5, 2014

The ACUTE Innovations Modular RibLoc System (RibLoc U plus) is comprised titanium plates and screws that are used to…

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

ACUTE Innovations, LLC

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2014

Walmart Great Value Tex Mex Trail Mix, Net Wt 28 oz (793g), Distributed by Wal Mart Stores, Inc., Bentonville, AR,…

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

Ann's House

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2014

Simplexa Flu A/B & RSV Direct assay, Model MOL2650. The Focus Diagnostics Simplexa Flu A/B & RSV Direct assay is…

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

Focus Diagnostics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2014

Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by…

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

Kimberly-Clark Corporation

FDA (openFDA device 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.