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 Oct 10, 2018
EVERYBURGER - Burger-Shaped Chocolate Cookies: NET WT. 2.32 oz. (66 g) There are 2 packing sizes; 10 items per case and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wismettac Asian Foods (USA) dba Nishimoto Trading Co. Ltd.
FDA (openFDA food enforcement)
Reported Oct 3, 2018
ESSENTIO Pacemaker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Retractor System Elastic Stays (Part 3314-lG; 3316-lG; 3550-lG) Product Usage: The Retractor System Elastic Stays (Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Visualase Thermal Therapy System, Software: Visualase Software versions 3.1.1 - 3.2, Product #: 9735542
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Medtronic Clip Gun Magazines are packaged in individually sealed pouches and distributed in boxes containing 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
FDA (openFDA device enforcement)
Reported Oct 3, 2018
INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
26 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2018
PR1000 Pivot Rehab Bed AC powered adjustable bed.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Med-Mizer, Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2018
Endoscopic Cleaning Brush, single use, sold in kits and labeled as the following: a. Item Number DYK1002DCB, BRUSH,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2018
PATHFAST Myoglobin II reagent cartridge Catalog Number: PF1111-K PATHFAST¿ NTproBNP is a product for in-vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymedco, Inc.,/Polymedco Cancer Diagnostic Products, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2018
White Corn Tortilla Chips packaged under the following brand names and sizes: 1. Shearer's White Restaurant Style Bulk,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shearers Foods, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 19, 2018
Dewey's BAKERY Soft Baked TRIPLE CHOCOLATE BROWNIE COOKIES NET WT. 6 OZ paper bag Dewey's BAKERY WINSTON-SALEM, NC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dewey's Bakery, Inc. dba Salem Baking Company
FDA (openFDA food enforcement)
Reported Sep 19, 2018
da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. 420179-16 Product Usage: EndoWrist Instruments,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 19, 2018
Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 280 mm, Item Number: 814309280
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
128 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2018
DRAD-3000E (Radrex-i) TFP-4336W (Wireless FPD)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 5, 2018
Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Pads. Product Packaging: Three (3) PVP-I prep pads…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Medical Division
FDA (openFDA device enforcement)
Reported Sep 5, 2018
equate High Performance Protein Shake: Chocolate, Naturally & Artificially Flavored, ready to drink; 11 FL OZ (325 mL),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.California Natural Products
FDA (openFDA food enforcement)
Reported Sep 5, 2018
Stryker Mako Vizadisc Knee Procedure Tracking Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 5, 2018
Tomato Condensed Soup, 26 oz (1 LB 10 OZ) 737 g, 307 x 512 Can, Family Size, 12 cans per tray, shelf stable
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Morgan Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 29, 2018
BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
CAREstream ProNox Nitrous Oxide Delivery System labeled as the following: a. CMI-0100 PNX, Pro-Nox Mixer - Canadian; b.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CAREstream Medical LLC
FDA (openFDA device enforcement)
Reported Aug 29, 2018
BEST TASTE BRAND SNACK GINGER SLICED, Net Weight 200g, 7 OZ, Distributed by; COUNTRY FAVOR., INC U.S.A; PRODUCT OF…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Country Favor Inc.
FDA (openFDA food enforcement)
Reported Aug 29, 2018
ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Peanut Paste/Butter bulk tankers
High riskUsing this product could cause serious injury, illness or death — stop using it now.Peanut Processors, 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.