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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 48,122 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.

Medical devices

Reported Nov 18, 2015

Stryker Radius 5.5 to 3.5 Rod to Red Connector, REF 48664530. Intended to provide additional support during fusion…

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

Stryker Spine

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2015

SSS Reprocessed Zimmer, Synthes, Stryker and Linvatec Drill Bits and Blades Surgical drill bits, blades, burs, chisels,…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2015

Synthes Small Notch Titanium Reconstructive Plate set (SNTRP). Ti PLATE/ROD/PLATE 231mm 6HOLES/5.0mm ROD/17HOLES.…

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

Synthes (USA) Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2015

ARROW PICC Kit featuring Chlorag+ard Technology Midline Catheterization Kit ARROW Advantage5 Pressure Injectable PICC…

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

Arrow International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2015

EnVision FLEX/HRP visualization reagent found in the following kits: EnVision FLEX, High pH (Link) EnVision FLEX+,…

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

Dako North America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2015

Robotic Arm Interactive Orthopedic (RIO) system component PN#205143 (locking pin) and PN# 112220 (connector). Indicated…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2015

Medtronic Achieve Cables, model 990066. The sterile, single use only Electrical Cable (Model 990066) provides the…

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

Medtronic Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 11, 2015

ON THE BORDER MEXICAN GRILL & CANTINA Cafe Style Tortilla Chips 18 oz. bags

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

Shearer's Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 4, 2015

Exprt Precision System: Revision Knee, Model Number 160-010-726/738 For use with the Exprt Knee System in total knee…

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

Encore Medical, LP

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 4, 2015

CC cartridges for IRMA TRUPOINT Blood Gas Analyzer, PN 039903. The CC Cartridge are single use, disposable, in vitro…

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

LifeHealth, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 4, 2015

Brilliance 16-Slice (Air) Computed Tomography X-ray systems. Intended to produce cross-sectional images of the body.

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

Philips Medical Systems (Cleveland) Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2015

All Philips Ingenia, Intera, Achieva and Multiva MR systems using R5.1i and R5.1 .2 version of software. Indicated for…

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

Philips Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2015

Monode, Shortwave Accessory Model #: 02200002 Used in conjunction with the Intelect Shortwave Diathermy 100 and…

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

Djo, LLC

FDA (openFDA device enforcement)

Food

Reported Oct 21, 2015

GoGo SQueeZ Applesauce, Apple Apple, individually wrapped in foil pouch in cardboard carton; sizes include: 4-pack,…

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

Materne, North America

12 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 21, 2015

French Burnt Peanuts, NET WEIGHT 8 OZ (227g) Old Time Candy.com Distributed by Old Time Candy Company LaGrange, OH…

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

Old Time Candy

FDA (openFDA food enforcement)

Medical devices

Reported Oct 14, 2015

Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including…

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

GE Healthcare

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2015

Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.

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

Lifeline Systems, Incorporated

FDA (openFDA device enforcement)

Food

Reported Oct 7, 2015

Imperial Sugar, Pure Granulated Sugar, Net wt. 50 lbs (22.6 kg), Distributed by Imperial-Savannah LP, Sugar Land, Texas…

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

Savannah-Imperial LP- Savannah Sugar Refinery

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 7, 2015

Histolock Resection Device, US Endoscopy. An electrosurgical device designed to be used to endoscopically grasp,…

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

US Endoscopy Group Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2015

The Leica ASP6025 Tissue Processor. Pathology and Hematology Departments. The Leica ASP6025 Tissue Processor is an…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 30, 2015

Sam Mills Gluten Free Chocolate Chip Granola Bars with Dark Chocolate 5 bars/4.4oz Box (0.88oz each bar)

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

Sam MillsUSA LLC

FDA (openFDA food enforcement)

Food

Reported Sep 23, 2015

KellBran" CANDIES, INC. creamy rich caramel popcorn Net Wt. 8 oz. (226.64 Grams) ALLERGY INFO: Manufactured in a…

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

Kellbran Candies and Snacks Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2015

Temporary Total Artificial Heart (TAH-t) with Freedom Driver System REF 595000-001 Product Usage: Freedom Drivers are…

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

SynCardia Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2015

MEDIVATORS HEMOCOR HPH700, HPH-1400TS, HPH-1000TS. Enables the perfusionist to manage the patient's hematocrit and…

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

Medtronic Perfusion Systems

1 more product in this recall

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.