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 48,828 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.

Medical devices

Reported Apr 3, 2013

KIMGUARD Container Filters, 7.5in (19cm), Round and 9in. X 9in. (23cm x 23cm), Square. Intended to be used to enclose…

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

Kimberly-Clark Corporation

FDA (openFDA device enforcement)

Drugs

Reported Apr 3, 2013

PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Phenylephrine HCL 325/10/5 mg gel…

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

L. Perrigo Co.

FDA (openFDA drug enforcement)

Medical devices

Reported Apr 3, 2013

Siemens Axiom Artis zeego systems with software version VC14, VC20 and VC21 in conjunction with specific technical…

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 Apr 3, 2013

Synthes Dens Instrument Set (Dens Graphic Case), Part Number 687.030 (also known as the Anterior Column Retractor Set)…

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

Synthes USA HQ, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Apr 3, 2013

Ciprofloxacin Tablets USP, 500 mg, 100-count bottle, Rx only, Manufactured for West-ward Pharmaceutical Corp.,…

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

West-ward Pharmaceutical Corp.

FDA (openFDA drug enforcement)

Food

Reported Mar 27, 2013

Great Value All Natural Mild Chunky Salsa, 24 oz (1-lb 8-oz) 680 g.; UPC 007874208639; Distributed by: Wal-Mart Stores,…

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

Conagra Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 27, 2013

Vascular Solutions, Inc., Guardian II and Guardian II NC Hemostasis Valve, used in cardiopulmonary bypass. Model…

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

Vascular Solutions, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 20, 2013

10021 Roman Meal Premium Oat Bran Mix ( Oat Flour, Oats, Oat Bran, white Wheat Bran, Red Wheat Bran, Stabilizi....,…

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

Dakota Specialty Milling, Inc.

51 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 20, 2013

Brilliance 6, 10, 16, 40, 64, Big Bore and the iCT, iCT SP, Ingenuity CT and MX8000 Dual v. EXP are Computed Tomography…

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)

Medical devices

Reported Mar 13, 2013

PSX PROXIMATE Skin Staple Extractor, ETHICON ENDO-SURGERY, LLC. For routine skin closure in a wide variety of surgical…

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

Ethicon Endo-Surgery Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 13, 2013

GE Healthcare Volume Viewer Plus 5.x (Advantage Workstation 4.2) Volume Viewer 3.x (Advantage Workstation 4.1) Volume…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 13, 2013

Chocolate bridge mix in 10 oz, 3 oz, and 3.5 oz bags

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

Gorant Candies Inc. A Division

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 13, 2013

AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization of heat and moisture-stable materials used in…

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

Steris Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2013

Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.

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

Aesculap, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2013

Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by Philips Medical Systems, Highland Heights, OH…

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

Philips Medical Systems (Cleveland) Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2013

Whole Foods Market Whole Catch Wild Alaskan Sockeye Smoked Salmon, Cold Smoked Sliced, Net Wt. 4 oz, Distributed by…

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

Whole Foods Market

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 27, 2013

Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous…

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

Animas Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2013

Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and…

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

Hill-Rom, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2013

MAYFIELD¿ Composite Series Base Unit Standard, Model (A3101), Rx ONLY, Integra LifeScience Corporation, 4900 Charlemar…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Food

Reported Feb 27, 2013

Lean Cuisine Culinary Collection Mushroom Mezzaluna Ravioli ravioli filled with portobello & button mushrooms, romano &…

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

Nestle USA

FDA (openFDA food enforcement)

Medical devices

Reported Feb 27, 2013

Vascular Solutions, SuperCross Microcatheter, Sterilized using ethylene oxide, Rx Only, Model numbers 5300 - 5307,…

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

Vascular Solutions, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 20, 2013

Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar.

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

Mizuho OSI

FDA (openFDA device enforcement)

Medical devices

Reported Feb 20, 2013

St. Jude Medical, AGA Medical corporation, AMPLATZER¿ TorqVue¿ FX Delivery System. Model #'s: 9-ITVFX06F45/60,…

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

St Jude Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2013

Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the…

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

Diagnostic Hybrids Inc.

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.