All recall categories

Recalls distributed in Arkansas

These notices name Arkansas 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.

2,558 stored notices name Arkansas, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.

Medical devices

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)

Medical devices

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)

Medical devices

Reported Apr 5, 2017

AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for use in providing diagnostic quality images to…

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

AGFA Healthcare Corp.

FDA (openFDA device enforcement)

Food

Reported Apr 5, 2017

Truco 1 50/50 Corn Masa Flour 50 lb bags & totes

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

Azteca Milling LP

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

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)

Food

Reported Apr 5, 2017

The product is packaged in a white plastic bottle with green lettering. The label reads in part "LIFE RISING DHZC-2,…

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

Life Rising Corp. S

FDA (openFDA food enforcement)

Medical devices

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)

Medical devices

Reported Mar 29, 2017

Poly Component Trial, MPCS, packaged in the following sizes and configurations: a) Poly Component Trial - MPCS 3x10L,…

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

Medtronic Sofamor Danek USA Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 29, 2017

Brilliance BigBore Oncology CT - 728243 Computed Tomography X-ray systems intended to produce cross-sectional Images of…

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

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

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)

Medical devices

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)

Medical devices

Reported Mar 22, 2017

BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01

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

Medtronic

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 22, 2017

Terumo Advanced Perfusion System 1-Level Sensor II Pads, Product Usage: Ultrasonic couplant used to facilitate the…

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 Mar 15, 2017

McCormick & Co., Inc., Stubbs Barbecue. 18oz Best By Date of January 17, 2020.

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

McCormick & Co. Inc. Spice Mill Plant

FDA (openFDA food enforcement)

Medical devices

Reported Mar 15, 2017

Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,

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

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

BD AffirM VPIII Microbial Identification Test

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers…

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

Cook Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

EliA Sample Diluent, Article number, 83-1023-01

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

Phadia US Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 1, 2017

ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 ETEST is a quantitative technique for determining the…

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported Mar 1, 2017

Oxford Knee System Tibial Resector Body Tube & Guides Product Usage: Instruments for use with the Oxford Uni Partial…

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

Biomet U.K., Ltd.

23 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 1, 2017

Golden Flake (R) HOT THIN & CRISPY POTATO CHIPS, NET WT. 5 OZ. (141.8g), Golden Flake Snack Foods, Inc., Birmingham, AL…

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

Golden Flake Snack Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Mar 1, 2017

A) Palmer's Candies Chocolate Almond Bark , NET WT 9 OZ (255 g) packaged in plastic clamshell container, UPC…

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

Palmer and Company, dba Palmer Candy Co.

17 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 1, 2017

Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.

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

Tosoh Bioscience, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 1, 2017

GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The GrebSet micro-introducer…

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

Vascular Solutions, Inc.

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.