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.
Reported Apr 15, 2015
Instrument Kit for use with OsteoSponge SC grafts. The Instrument Kit is used to insert OsteoSponge SC grafts to fill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bacterin International, Inc.
FDA (openFDA device enforcement)
Reported Apr 15, 2015
CS 8100, CATALOG # (s): 5303045, 5311129, 5303060, 5303110 Intended to produce complete or segmented tomographic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 15, 2015
Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Apr 15, 2015
Texamerican Chili Powder: 5 lbs. Item Number: ARCH064-50; 10 lbs. Item Number: TF5002 (R&D only).
High riskUsing this product could cause serious injury, illness or death — stop using it now.Texamerican Food Blending, Inc.
7 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 8, 2015
Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc. Cardiac Rhythm Disease Management
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Vitagel; indicated in surgical procedures (other than in neurosurgical and ophthalmic) as an adjunct to hemostasis when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthovita, Inc., dba Stryker Orthobiologics.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence technology, Brilliance iCT, Brilliance iCT SP,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm; The 130 Degree Aiming Arm and 125 Degree Aiming Arm are a part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Mini Naan Eight (8) nann packaged in coated paper printed board and transparent wrap with a net weight of 12.6 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.fgf brands, Inc.
FDA (openFDA food enforcement)
Reported Apr 1, 2015
Whole Foods Market "Chocolate Cake for Two" UPC code: 246357004999 Net Wt. 11 oz (0.69lb) in a clear plastic "clam…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Food Market
FDA (openFDA food enforcement)
Reported Mar 25, 2015
Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or…
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)
Reported Mar 25, 2015
CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Mar 18, 2015
Apollo (cold) Laser Desktop Control Units, Model AP2-DT. The Apollo IR Heat Lamp System is intended to emit energy in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pivotal Health Solutions
FDA (openFDA device enforcement)
Reported Mar 11, 2015
DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.iCAD, Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2015
Adams Pantry Basics Chili Powder Net Wt. 2.82 oz (80 g) UPC: 041313017224; Adams Pantry Basics Value Size Chili Powder…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Adams Extract & Spice LLC
44 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 4, 2015
Starburst MRI Semi-Flex Electrode Device, 25cm/Attached Cable/14Ga/6.4F, Product No. H7877001039091, Catalog No.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics
FDA (openFDA device enforcement)
Reported Mar 4, 2015
The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare…
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)
Reported Mar 4, 2015
TDX Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 4, 2015
Philips Multi Diagnost Eleva II
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 4, 2015
CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2015
Sunset Farm Foods, Inc Recalls Sausage Products Due To Misbranding And Undeclared Allergen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sunset Farm Foods, Inc.
USDA FSIS
Reported Feb 25, 2015
Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use with the Robotic Arm Interactive Orthopedic System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Feb 25, 2015
Terumo HX2 Temperature Management System provides temperature control of two independent water circuits that directly…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
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.