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

Medical devices

Reported Jun 11, 2014

ExacTrac 5.5, an Image Processing System used for patient positioning for radiation therapy or radiosurgery.

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

Brainlab AG

FDA (openFDA device enforcement)

Medical devices

Reported Jun 11, 2014

BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive (BioGlue) is indicated for use as an adjunct to…

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

CryoLife, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 11, 2014

Integra Newdeal SURFIX Fixed Angle Locking Screw 3.5mm x 22mm (catalog number 285322S) and 3.5mm x 30mm (catalog number…

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

Integra LifeSciences Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 11, 2014

The Stryker NAV3i Platform is a mobile cart platform consisting of the sub-components Stryker Nav3 Graphite Camera,…

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 Jun 4, 2014

ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35); ultrasound imaging system.

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 May 28, 2014

GE Healthcare, NeuroMuscular Transmission Module, E-NMT-01 Product Usage: The Datex-Ohmeda S/5TM E-NMT module is…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 28, 2014

LATEX-FREE; EXTENSION SET; For Bladder Irrigation or Urinary Drainage, Compatible with T-U-R FLOW-POUCH RESERVOIR, list…

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

Hospira Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 21, 2014

Private Selection Chocolate Hazelnut Mascarpone Ice Cream, 16 fl oz lamented carton. Product labeled in part, "PRIVATE…

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

Kroger Co.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 21, 2014

Syngo Dynamics v9.5 system. A Picture Archiving and Communication System (PACS) intended for acceptance, transfer,…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported May 14, 2014

PRIVATE SELECTION SWEET STRAWBERRY SORBET, Labeled in part: "INGREDIENTS: WATER, SUGAR***DISTRIBUTED BY, THE KROGER…

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

Kroger Co.

FDA (openFDA food enforcement)

Medical devices

Reported May 14, 2014

Mar Cor Purification, Central Water Platform (CWP), 102, 104 and 106. Product Usage: The CWP is a Central reverse…

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

Mar Cor Purification

FDA (openFDA device enforcement)

Medical devices

Reported May 7, 2014

Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions including whole blood or red blood cell…

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

Hospira Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2014

Amo-O Herbal Stimulator, 2 fl. oz. Manufactured by Meta Labs, Alpharetta, GA 30076, UPC Code 80702-1 Product Usage: The…

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

Altasource LLC dba Meta Labs LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2014

ZYM B Reagent (REF 70493). The ZYM B reagent is an additional test used to reveal the results of some miniaturized…

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

BioMerieux SA

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2014

VITROS Chemistry Products CDM PROM (Calibration Data Module) No. 0168, Catalog Number/REF 199 9077, used in conjunction…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2014

Stryker PenAdapt"; Rx Only, Sterile. This device is an accessory to an electrosurgical unit (ESU). The PenAdapt is used…

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2014

SmartSite Extension Set, Model No. 20029E, intravascular administration set.

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 23, 2014

Luna Chocolate Chunk; Whole Nutrition Bar for Women; 15 count box. Clif Bar & Company, Emeryville, CA

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

Clif Bar And Company

FDA (openFDA food enforcement)

Medical devices

Reported Apr 16, 2014

7mm Drain Kit, Flat Full Perforated, Saber 100ml Bulb and 3C System Sterile (10/case) Intended for closed wound suction…

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

Aspen Surgical Products, Inc.

18 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 16, 2014

Prego Italian Sauce Traditional, NET WT. 24 OZ (1 LB. 80 Z.)(680 g) in glass jars.

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

Campbell Soup Supply Co., LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 16, 2014

Reusable latex breathing bags with multiple part numbers and sold as part of test lung part number and reusable…

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

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 9, 2014

Ideal Protein Double Chocolate Brownie. Individually wrapped, sold in boxes of 7.

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

Laboratories Cop Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 9, 2014

Pinnacle3 Radiation Therapy Planning (RTP) System, software version 9.0.

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

Philips Medical Systems (Cleveland), Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 9, 2014

Artis Zee Angiographic x-ray systems.

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

Siemens Medical Solutions USA, 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.