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 48,784 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
Reported Jul 27, 2016
Kellogg's Special K Mini Brownies Blondie, 6 ct, 4.44 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellogg Company
24 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2016
Syngo.via, picture archiving and communications system software controlled. Intended to be used for viewing,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2016
OT1000 Series Orthopedic Surgical Tables
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw Guide Sleeve, Surgical Instrument Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Jul 27, 2016
HX2" Temperature Management Systems; The Terumo¿ HX2" Temperature Management System provides temperature control of two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
Mammotome Revolve Dual Vacuum Assist Biopsy System Model number: MST1009 & MST0815. Each disposable probe is packaged…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Devicor Medical Products Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through…
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)
Reported Jul 20, 2016
6.5 mm Cannulated Screw, Product code HWC, Device Listing Number D028949, Screw, Fixation Bone Product Usage: Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
Kroger SALAD TOPPERS Roasted & Salted Sunflower Kernels NET WT 3.5 OZ (99G) INGREDIENTS: SUNFLOWER KERNELS, COTTONSEED…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 14, 2016
Haring Catfish, Inc. Recalls Siluriformes Fish Products Due To Possible Adulteration
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haring Catfish
USDA FSIS
Reported Jul 13, 2016
The System 83 Plus, Endoscope Washer/Disinfector Designed for the simultaneous reprocessing of up to two flexible…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Custom Ultrasonics, 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.