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.

Medical devices

Reported Feb 1, 2017

Hitachi Oasis MRI System - C-Spine Coil

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 Feb 1, 2017

SCC Soft Computer Softbank II software Product Usage: Supports single and multi-site transfusion services in healthcare…

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

Soft Computer Consultants, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2017

Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.

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

Villa Radiology Systems LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 25, 2017

NO EGG CHOCOLATE CHIP COOKIE DOUGH 03-3014, Net Weight 30 lb (13.61 Kg) Aspen Hills, Inc. Garner, IA 50438

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

Aspen Hills, Inc.

18 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 25, 2017

Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 The Halo One Thin-Walled Guiding Sheath is designed to perform…

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

Bard Peripheral Vascular, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 25, 2017

Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version Number: V3.16.13.0 Intended for use as a…

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

Dicom Grid Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 25, 2017

Monaco RTP System. Used to make treatment plans for patients with prescriptions for external beam radiation therapy.

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 25, 2017

Novation Cemented Plus Femoral Stem, 12/14, Collared, Standard Offset, Matte, Cemented, Size 15.

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

Exactech, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 25, 2017

PREMIER EHEC and PREMIER EHEC Bulk.

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

Meridian Bioscience Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 25, 2017

Kabayaki Unagi Bits (Broiled Eel Bits) Tetsujin

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

Ming Hong International,Inc.

FDA (openFDA food enforcement)

Food

Reported Jan 25, 2017

Delizza Patisserie, Belgian Custard Cream Mini Eclairs, Net Wt. 420g  14.8 oz., UPC Code: 6 76670 00106 9(30 count)…

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

Poppie International Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 18, 2017

Biscuits & Gravy Seasoning CR/ Barrel O' Fun. Product Code: T3669. 50 lb bags

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

All American Seasonings, Inc.

25 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 18, 2017

In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY…

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

Brand Castle LLC

FDA (openFDA food enforcement)

Food

Reported Jan 18, 2017

Country Gardens Cuisine, Singles, Broccoli Cheese Soup with Rice, Net Wt. 1.25 oz (35 grams)

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

Copperleaf Kitchen, LLC Comfort Foods Division

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2017

OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the…

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

GE OEC Medical Systems, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2017

Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jan 18, 2017

Testosterone Cypionate 200 mg/mL in Sesame Oil, 4 mL and 5 mL vials, Rx only, For IM injection, Pharm D Solutions, Loop…

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

Pharm D Solutions, LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 18, 2017

Biograph mCT S(40)-3R, Material Number 10248668 The Siemens Biograph mCT and Biograph mCT Flow systems are combined…

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

Siemens Medical Solutions USA Inc.

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2017

Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as…

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

Stryker Sustainability Solutions

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 11, 2017

G3 Opticage Expandable Interbody Fusion Device, Model No. 9180-00, 9180-01, 9180-06, 9180-07, 9180-17, 9101-00, 9101-06…

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

Interventional Spine Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 11, 2017

Winco Foods Creamy Ranch Dressing 16 fl oz. UPC Code: 0 70552 70103 8

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

Vanlaw Food Products, Inc.

FDA (openFDA food enforcement)

Drugs

Reported Jan 4, 2017

INOVA (benzoyl peroxide) 4%, Easy Pad (tocopherol) 5%, For topical use only, packaged in a box containing: 30 pads of…

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

Cipher Pharmaceuticals US LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 4, 2017

Innova 2000

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

GE Healthcare, LLC

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 4, 2017

Specimen Gate Laboratory 5002-0180, Specimen Gate eReports 5002-0370, Software Version 1.0 Specimen Gate Laboratory is…

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

PerkinElmer Health Sciences, 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.