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.
Reported Apr 6, 2016
Synthes Interlocking Bolt, 151 mm (General and Plastics Surgery Devices) Guide, Surgical Instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC, Size 3 - Catalog # AR-503-TTTD, Size 4 -Catalog #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Siemens ADVIA Centaur Enhance Estradiol Test Code eE2 Catalog Number: 10490889, 10491445, 10697757 Product Usage: For…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Universal Clamp¿ System (IFU reference: SNA027-N-90001). Provides the stability required for solid bone fusion and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Spine, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 23, 2016
McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 11.9 and McKesson Radiology (MR) products…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System Accu-Chek inform II…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS) Model Numbers: 10091805, 10091807, 10091637,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Super Arrow-Flex Percutaneous Sheath Introducer Sets REF CL-07035 or CL-07635 or CL-07735 or CL-07835 Super Arrow-Flex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Bertolli Extra Virgin Olive Oil, 8.5 oz. and Carapelli Extra Virgin Olive Oil, 25.5 oz., packaged in glass bottles.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.DEOLEO USA, Inc.
FDA (openFDA food enforcement)
Reported Mar 16, 2016
Asiago Cheese Sauce Seasoning NET CONTENTS: 44.3 POUNDS 20.1 KILOGRAMS packed in flexible bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Illes Food Ingredients Ltd.
FDA (openFDA food enforcement)
Reported Mar 16, 2016
Mobile wDR motorized portable diagnostic X-ray systems. Intended for use by a qualified/trained doctor or technologist…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal S.A.
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E - 2-Pack Catalog Number: 04634452 SMN: 10309079 ADVIA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 16, 2016
ROTROL P Control for ROTEM delta Thromboelastometry System, For In Vitro Diagnostic Use Only. Quality control material…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TEM Systems Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2016
Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended to spray liquids in aerosol form into gasses…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2016
BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2016
This reagent is for in vitro diagnostic use. Pax-5 (1EW) monoclonal antibody is intended to be used for the qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2016
software for Syngo Dynamics 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.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2016
Synthes Small Electric Drive (SED)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Feb 24, 2016
RED DIAMOND, COLOMBIAN, NATURALLY CAFFEINATED, Coffee Concentrate, Mix Ratio 69 + 1, Net contents 1/2 Gallon,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Red Diamond, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 24, 2016
High Flow Irrigation Extender; Part Number 72201021. Arthroscopic accessories are indicated for use in access of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc., Endoscopy Div.
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet France SARL
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Arctic Sun 5000 and Arctic Sun 2000; Intended for monitoring and controlling patient temperatures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, 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.