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.

2,595 stored notices name Arkansas, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.

Medical devices

Reported Mar 25, 2015

Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2015

CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.

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

Smiths Medical ASD, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2015

Apollo (cold) Laser Desktop Control Units, Model AP2-DT. The Apollo IR Heat Lamp System is intended to emit energy in…

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

Pivotal Health Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2015

DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2

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

iCAD, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 4, 2015

Adams Pantry Basics Chili Powder Net Wt. 2.82 oz (80 g) UPC: 041313017224; Adams Pantry Basics Value Size Chili Powder…

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

Adams Extract & Spice LLC

44 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 4, 2015

Starburst MRI Semi-Flex Electrode Device, 25cm/Attached Cable/14Ga/6.4F, Product No. H7877001039091, Catalog No.…

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

Angiodynamics

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2015

The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare…

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

Hospira Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2015

TDX Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width…

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

Invacare Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2015

Philips Multi Diagnost Eleva II

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

Philips Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2015

CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of…

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

Zimmer GmbH

4 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 26, 2015

Sunset Farm Foods, Inc Recalls Sausage Products Due To Misbranding And Undeclared Allergen

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

Sunset Farm Foods, Inc.

USDA FSIS

Medical devices

Reported Feb 25, 2015

Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use with the Robotic Arm Interactive Orthopedic System…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2015

Terumo HX2 Temperature Management System provides temperature control of two independent water circuits that directly…

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

Terumo Cardiovascular Systems Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2015

The MAYFIELD¿ Ultra 360 Base Unit for head positioner, one unit per package. Product Usage: This product provides the…

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

Integra LifeSciences Corporation

FDA (openFDA device enforcement)

Food

Reported Feb 18, 2015

MorningStar Farms Spicy Black Bean Burger: 9.50 oz (4 ct) - UPC 2898939207; 18.90 oz (8 ct): UPC 2898971750; 8.7 lb…

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

Kellogg USA Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 18, 2015

VisiPlugST for the Lacrimal Efficiency Test. It is also sold in the EU as CollaSyn Plugs. Model number 1813, 1814,…

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

Lacrimedics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2015

MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm; Part Number 86001; Lot Numbers A1405048, A1404026 Product Usage:…

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

Stryker Craniomaxillofacial Division

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2015

System 6 Aseptic Housing. The Stryker System 6 Aseptic Housings provide a sterile enclosure for the Stryker Non-sterile…

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

Stryker Instruments Div.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2015

Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients.

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

Virtual Imaging, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 11, 2015

Baxter Integrated APD Set with Cassette 3-Prong, Sterile, nonpyrogenic fluid path. Product Usage: The recall device is…

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

Baxter Healthcare Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 11, 2015

Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is…

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

Cardinal Health

FDA (openFDA device enforcement)

Food

Reported Feb 11, 2015

Dried Bean Curd Satay Flavor, 24x150g, Item No. 8533.

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

Gemini Food Corporation Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 11, 2015

ABL90 FLEX analyzer; Model number 393-090. A portable, automated analyzer that measures pH, blood gases, electrolytes,…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 11, 2015

MobileDiagnost wDR motorized portable diagnostic X-ray systems.

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

Sedecal S.A.

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.