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 48,828 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.
Reported Aug 22, 2012
GE Healthcare Advantage Workstations, Advantage Worksation version 4.2 and 4.3 with Volume Viewer 2 (version 6.4-6.8)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 15, 2012
djo surgical Screw 6.5 mm, Sz 25mm, low profile. Product is intended for the fixation of the acetabular shell or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Aug 15, 2012
Crispy By TWI Foods Punjabi Cookies Just Baked Product of Canada 2600 Drew Road, Mississauga, ON Canada L4T 3M5 Net Wt.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fahman Enterprises, Inc.
FDA (openFDA food enforcement)
Reported Aug 15, 2012
The ABL software version 6.12 for the ABL800 analyzer. The analyzers are intended for the in Vitro testing of: -Samples…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Defense Nutrition Warrior Whey Natural Powder, dietary supplement, packaged in 14-oz. bottles and packed 6/14-oz…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Defense Nutrition
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 8, 2012
Integra¿ Advansys Medial Lisfranc Plate (MLP), Integra, 311 Enterprise Drive, Plainsboro, NJ 08536 The Advansys plates…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Aug 8, 2012
The Reliance 130 and 130L Cart Washer/Disinfector is a high capacity mechanical washer intended for use in the washing,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Aug 1, 2012
PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tripath Imaging, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Infusomat(R) Space Pump (US Version) with software version 686G030103 (commonly termed 'G03'), 686E030003, 686F030005,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Philips Brilliance 6, 16, 40, 64, Big Bore, iCT and iCT SP are Computed Tomography X-Ray Systems. The devices are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360 Tablets, Proprietary Blend:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Standard Process, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 25, 2012
Terumo Advanced Perfusion System 1 System 1 Base, 100/120V. The Terumo Advanced Perfusion System 1 is indicated for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 18, 2012
Jimmy Peppers Hot Cherry Sliced Peppers, 1 gallon plastic jars
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cosmo's Food Products, Inc.
FDA (openFDA food enforcement)
Reported Jul 18, 2012
Tom's Bacon Cheddar Fries, Flavored Corn and Potato Snacks, Net Wt., 2.75 oz (78.0g),
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snyder's - Lance Inc.
FDA (openFDA food enforcement)
Reported Jul 18, 2012
superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated for use for displaying images of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.superDimension, Inc.
FDA (openFDA device enforcement)
Reported Jul 11, 2012
TDX SP Power Wheelchair, TDX SR Power Wheelchair, TDX SI Power Wheelchair. Model Number(s): TDXSI, TDXSI-2, TDXSI-2-S,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Jul 4, 2012
ARCHITECT CA 19-9XR Reagent Kit; ARCHITECT CA 19-9 Reagent Kit, list 291-20 (4 x 100 tests), 2K91-25 and 2K91-27 (1 x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Jul 4, 2012
BCS(R) Behring Coagulation System, Device catalog No. OVIO03 Product Usage: Multipurpose system for In Vitro…
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)
Reported Jul 4, 2012
Sarns Antegrade Cardioplegia Cannula: ROOT INFUSTION VENT CATHETER WITH 12 GAUGE BLUE NEEDLE RECTANGULAR FLANGE, 6" (15…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
19 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 27, 2012
Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Jun 27, 2012
Diced Red Onions, 7oz clear plastic clamshell labeled Gills Onions with the May 17, 2012 use by date, United States UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gills Onions, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 27, 2012
Olympic Cool-Cap System is intended to provide treatment for neonatal hypoxic-ischemic encephalopathy (HIE). The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Jun 27, 2012
SARNS HIGH-FLOW AORTIC ARCH CANNULA: 5.2 MM (16 FR) 00 WITH 3/8" CONNECTOR, 7.5" (19 CM) LONG. The Sarns High Flow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
10 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 20, 2012
AlsoSalt Sodium Free Butter flavored Salt Substitute, 2.5 oz. bottle
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diversified Natural Products, Inc.
FDA (openFDA food 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.