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.

Food

Reported Dec 25, 2013

Nature's Way, UPC 33674149263, Alive Whole Food Energizer with Iron, 60 Tabs 20009807; Nature's Way, UPC 33674149270,…

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

Schwabe North America, Inc.

12 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2013

Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is an in vitro diagnostic test intended to…

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

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2013

Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion Pumps are designed for use in care areas for…

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

Smiths Medical ASD, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2013

VerifyNow IIb/IIIa Test, 10-Test Kit, Catalog No. 85310, 10 tests/box; 690 total tests. The VerifyNow IIb/IlIa Test is…

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

Accumetrics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2013

AMSCO¿ Evolution¿ steam sterilizer Transfer Carriage. Product Usage: Mobile, wheeled transportation unit utilized to…

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

Steris Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2013

Helion S Exam Light or H300 The device is intended to locally illuminate an examination area of the patient's body with…

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

Trumpf Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 11, 2013

Crunch Pak Apple Slices with Low Fat Caramel Dip, 5/2.5 oz. Tart with Caramel Sauce. The clamshell includes 5/2 oz.…

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

Crunch Pak, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 11, 2013

Product #4124: Caramel dip in plastic containers

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

Gold Medal Products

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 4, 2013

Baxter, VIAL-MATE Adaptor, 2B8071, Rx Only, STERILE R, Baxter Healthcare Corporation, Deerfield, IL 30015 USA The…

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

Baxter Healthcare Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2013

SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED SIZE 1-1.5 HP M.B.T. Keel Punch Knee Instrument is used to…

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

DePuy Orthopaedics, Inc.

11 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 4, 2013

Mozzarella String Cheese made with 2% milk for 1/4 less fat, sold under Kraft brand or Polly-O brand and packaged with…

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

Kraft Foods Group

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 27, 2013

The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the…

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 Nov 27, 2013

Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ, CGRLS190HS, CGRLS190S, CGRLS300HS, CGRLS300S. CGRXT190HJ,…

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

Medtronic Vascular

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2013

VITROS Chemistry Products ACET Slides, 90 slides/pack; catalog number 1037274 VITROS Chemistry Products ACET Slides…

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

Ortho-Clinical Diagnostics

36 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2013

SIGMA SPECTRUM Infusion Pump with Master Drug Library component (SHARP LCD screen, 55074-2 revision B) Product Usage:…

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

Baxter Healthcare Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2013

Carestream Vue PACS; VIRTUAL ACCESS SOFTWARE, WORKGROUP The CARESTREAM PACS is an image management system whose…

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

Carestream Health Inc.

49 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2013

Plum A+ Hyperbaric Infusion Pump; List Number 11005; Labeled in part: PLUM A+ HYPERBARIC; Product Usage: The Plum A+…

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

Hospira Inc.

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2013

Composite Series Skull Clamp, one clamp per tote. The MAYFIELD¿ Skull Clamp (A3059) is a cranial stabilization device,…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2013

Artis zee systems x-ray, angiographic 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 Nov 13, 2013

DRX Revolution, Catalog #'s 1)1019397, 2) 1023415 (w/ installation warranty, US-only) and 3) 1023423 (w/ parts…

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

Carestream Health Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2013

Adjustable Gastric Band, packaged alone in transparent PETG inner and outer blisters with Tyvek lids, or in various kit…

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

Ethicon Endo-Surgery Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 13, 2013

Jim Dandy¿ Iron Fortified Quick Grits, 1lb paper box, Labeled in part "INGREDIENTS: IRON, WHITE CORN GRITS, NIACIN,…

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

J M Smucker Co.

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2013

Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre; 15248C-22/25 The Regional Anesthesia family of products is…

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

Smiths Medical ASD, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2013

Harmony Equipment Management System, Model #603X/80XX, STERIS Corporation, Mentor, OH Harmony Equipment Management…

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

Steris Corporation

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.