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.
Reported Jul 19, 2017
The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended for cleaning and high-level disinfection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Chili Pequino 0.25 oz packaged in a clear plastic bag; Product Code 10106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bolner's Fiesta Products, Inc.
FDA (openFDA food enforcement)
Reported Jul 12, 2017
Drew Scientific DREW 3-PAC Reagent Kit containing: 5L Diluent, 750 mL Enzymatic Cleaner, and 125 mL Lysing Reagent.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.JAS Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Nussloch GmbH ASP6025 Tissue Processor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Electrophysiology catheter cables are designed as electrode cables with a multi-pin connector on the distal end and the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sterilmed Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2017
SHIMADZU Ceiling Type X-ray Tube Support CH-200/CH-200M Catalog Number: CH-200/CH-200M Holds an x-ray tube unit and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems USA Com
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 5, 2017
Kroger Dessert Cups yellow sponge cakes NET WT 6.5 oz (184g) INGREDIENTS: ***NONFAT M ILK***CONTAINS: WHEAT, EGGS, SOY.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
FDA (openFDA food enforcement)
Reported Jun 28, 2017
GEC TNT Thermanite 60 Capsules Dietary Supplement in clear plastic bottle, UPC: 689466706222.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genetic Edge Compounds LLC
FDA (openFDA food enforcement)
Reported Jun 28, 2017
PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE PASTE NET WT 4 OZ (113g) UPC 0 11110 80699 4…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Monfitello
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 28, 2017
Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 21, 2017
CADD¿ High Volume Administration Set with FlowStop, 21-7381-24. Product Usage: The CADD¿ High-Volume Administration set…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Jun 14, 2017
Beekley Medical 0-SPOT Mammography Skin Markers REF 652
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Beekley Corporation
FDA (openFDA device enforcement)
Reported Jun 14, 2017
Red Robin Burgers and Brews Crispy Onion Rings, frozen, Net wt. 14 ounce. Retail package UPC 0 43301 61119 3.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lamb Weston Inc.
FDA (openFDA food enforcement)
Reported Jun 7, 2017
Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported May 31, 2017
Ceftriaxone TX 32 US S30, Ref 412302 and Ceftriaxone TX 32 US F100, Ref 507058 ETEST is a quantitative technique for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported May 31, 2017
CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported May 31, 2017
Dip Trio Mix Homemade Gourmet Dip Mix Net Wt. 2.9 oz. Distributed by: Phoenix Food, LLC. Canton, TX 75103…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Phoenix Food, LLC
FDA (openFDA food enforcement)
Reported May 31, 2017
ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and Product Codes: (a) 12 OZ ARTISAN-STYLE PIZZA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rich Products Corp.
2 more products in this recall
FDA (openFDA food enforcement)
Reported May 24, 2017
Armour Eckrich Meats, LLC Recalls Ready-To-Eat Sausage Products Due to Possible Foreign Matter Contamination
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Armour Eckrich Meats, LLC
USDA FSIS
Reported May 24, 2017
SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 24, 2017
ETEST ETP32 (Ertapenem) Ref. 531640, 531600, blister packaging ETEST is a quantitative technique for determining the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported May 24, 2017
GIZA Vertebral Body Replacement
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eden Spine Europe SA
FDA (openFDA device enforcement)
Reported May 24, 2017
White OR Towels, X-Ray Detectable, Sterile, 4 Towels per/pk; 20pk/Cs. Intended for packing and absorption externally or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries Inc.
1 more product in this recall
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.