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 48,100 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.

Medical devices

Reported Aug 31, 2016

Infinite F50 instrument. The INFINITE F50 instrument is a 96-well absorbance reader for the measurement of light…

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

Tecan US, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 24, 2016

Bard TruGuide Disposable Coaxial Biopsy Needle  Mixed Product Part Number C1816B The TruGuide Disposable Coaxial…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 24, 2016

Summer Vegetable Salad with Seared Chicken, Garlic Croutons, and Mustard-Chive Vinaigrette

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

Hellofresh

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 24, 2016

Hospira RECEPTAL CANISTERS: 1L(1000mL), 1.5L(1500mL), 2L(2000mL) Canister, ATS, 2000, with Valve 1) List Numbers…

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

Hospira Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 24, 2016

VITROS Immunodiagnostic Products TSH Reagent Pack, REF/Catalog Number/Product Code 191 2997, Unique Device Identifier…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Aug 17, 2016

BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD); Catalog number 340383. Label states: Contains CD3 FITC/CD4 PE/CD45 per CP…

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

Becton, Dickinson and Company, BD Biosciences

FDA (openFDA device enforcement)

Medical devices

Reported Aug 17, 2016

NucliSENS easyMAG Magnetic Silica The NucliSENS easyMAG accessory products are reagents and disposable to be used with…

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

BioMerieux SA

FDA (openFDA device enforcement)

Food

Reported Aug 17, 2016

Williams Chipotle Chili Seasoning, Net Wt. 1 1/8 OZ. (32 g). Williams Foods, Inc. Lenexa, KS 66215. Packaged in paper…

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

CH Guenther & Sons, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 17, 2016

Healthwise, Protein Chips, Barbecue Crunch, Net Weight 1.2 ounces (34 grams), Distributed by Nutritional Resources,…

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

Nutritional Resources Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 17, 2016

MX 16-slice whole body computed tomography X-ray system. Imaging diagnostic tool.

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

Philips Medical Systems (Cleveland) Inc.

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 17, 2016

Synthes 2.4mm Titanium Locking Screws Self-Tapping with Stardrive Recess 12mm, Synthes 2.4mm Titanium Locking Screws…

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

Synthes (USA) Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2016

Spirit Plus Bed, A-C Powered Hospital Bed

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

CHG Hospital Beds Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2016

RePlant¿ Angled Abutment Part Number 6050-52-60

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

Implant Direct Sybron Manufacturing, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2016

Synergy Cranial S7. The software application is sent in CD format with an IFU, wrapped in plastic with a label for…

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

Medtronic Navigation, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2016

ONLINE TDM Vancomycin 100 tests; ONLINE TDM Vancomycin 200 tests; Hitachi Vancomycin (Modular P); Hitachi Vancomycin…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 10, 2016

Kroger DELUXE ICE CREAM S'MORES 48 FL OZ (1.5 QT) 1.4 ML INGREDIENTS: ICE CREAM***GRAHAM COOKIES***CHOCOLATE…

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

The Kroger Co.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 3, 2016

Babytherm 8004/8010, Infant Warmer, Class II device, 510 K K971198, Catalog # FR00105 (Babytherm 8010), 2M30404…

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

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2016

Stryker Orthopaedics Trident Constrained Liner Inserter/Impactor Tip, 22 mm, 28 mm, and 32 mm. Non Sterile Catalog…

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

Stryker Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

Amerigel Hydrogel Wound Dressing Advanced Formula for wound management 1 oz.

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

Amerx Health Care Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

BD Trucount Tubes: Catalog number: 340334 Hematology: BD Trucount tubes are used for determining absolute counts of…

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

Becton, Dickinson and Company, BD Biosciences

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2016

Mountain Thins Trail Mix flavor, packaged in a stand-up film pouch (resealable), net wt. 5.3 oz. The UPC is 0 41770…

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

Brown & Haley Inc.

FDA (openFDA food enforcement)

Food

Reported Jul 27, 2016

The sunflower kernels roasted and salted were packed in a 30 lbs. corrugated box with a poly liner with the following…

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

C.J. Dannemiller Company, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2016

Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS), Device Listing No.: D017878 is an in vitro diagnostic test…

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

CSL Behring GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

ATEC CANISTER. Suction Canister with Lid 490 cc., RX Only; Suction canister used to collect fluid during a breast…

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

Hologic, 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.