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.
Reported Apr 26, 2017
NEODENT CM Intraoral Scanbody, Article Number: 108.139
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instradent USA, Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
FDA (openFDA device enforcement)
Reported Apr 26, 2017
Buttermilk Powder, 25kg (BX25) Grade A
High riskUsing this product could cause serious injury, illness or death — stop using it now.United Dairymen
4 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 19, 2017
VIDAS Estradiol II, Ref 30431-01, 60 tests The VIDAS Estradiol II (E2 II) assay is intended for use on the instruments…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Apr 19, 2017
Boston Scientific Imager II Angiographic Catheter, M001316581 (5-pack outer package UPN), M001316580, single unit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Apr 19, 2017
ViperWire Advance Peripheral Guide Wire with Flex Tip, Model No. VPR-GW-FT18. Sterilized with Ethylene Oxide. The guide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported Apr 19, 2017
Specimen Gate Laboratory; Product Number: 5002-0180 Specimen Gate Laboratory is intended for use as a data processing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PerkinElmer Life and Analytical Sciences, Wallac, OY
FDA (openFDA device enforcement)
Reported Apr 19, 2017
Radiation Therapy Treatment Planning System, Model 4.5, 4.7, 5.0 RayStation is a software system designed for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Apr 19, 2017
CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Apr 12, 2017
Dark Chocolate bars Choklad Mork Dark Chocolate, Net Wt. 3.5 OZ. AND Chokland Mork Dark Chocolate 70%, Net Wt. 3.5 OZ.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ikea North America Srvcs Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 12, 2017
Mobile Diagnostic X-Ray System with Digital Panel
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare Inc.
FDA (openFDA device enforcement)
Reported Apr 12, 2017
BrightView SPECT model number 882480 BrightView and BrightView X are gamma cameras designed for single or dual detector…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 5, 2017
JResultNet drivers using ASTM coding language. Calculator/data processing module, for clinical use - Stand-alone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Data Innovations, LLC
FDA (openFDA device enforcement)
Reported Apr 5, 2017
Prosound F75 or F75 The Hitachi Aloka Medical, Ltd. Prosound F75 is intended for use by trained personnel (doctor,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Aloka Medical, Ltd.
FDA (openFDA device enforcement)
Reported Mar 29, 2017
MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Crossroads Extremity Systems LLC
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Strawberry Gelato, 5 Liter, 1 unit/case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dolce Dolci LLC dba Villa Dolce Gelato
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 29, 2017
Hitachi Oasis MRI System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Food City Colby Longhorn Cheese, 12 oz. package; also sold in random weight sizes. (Bashas' brand) sold at retail…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lakeview Cheese Co. LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 29, 2017
ATENOLOL Tablets, USP, 50 mg, 30-count bottle, Rx only, Distributed by: The Kroger Co., 1014 Vine Street, Cincinnati,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Legacy Pharmaceutical Packaging LLC
FDA (openFDA drug enforcement)
Reported Mar 29, 2017
Final Fit Software Version 1.11 and 1.12; PC Based software installed outside Nidek EC-5000 Excimer Laser System.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Raindrop Near Vision Inlay, Model# RD1-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Revision Optics Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Sargento Ultra Thin Sliced Longhorn Colby, 6.84 oz., UPC 4610000228, with Sell By dates of 12APR17B, 02FEB17F,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sargento Foods, Inc.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 29, 2017
Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is part of the Arial wireless emergency call…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stanley Security Solutions Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
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.