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.
2,591 stored notices name Arkansas, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.
Reported Jun 7, 2023
Elekta Medical Linear Accelerator (ELMA) included in the below platforms: a. Elekta Infinity; b. Versa HD; c. Elekta…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported May 31, 2023
Backpacker s Pantry Blueberry Peach Crisp, 4.6-ounce, packaged in a pouch, UPC-048143026143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Outdoor Products, Inc.
FDA (openFDA food enforcement)
Reported May 31, 2023
Copitas; small ceramic cups; "Del Maguey" embossed on the bottom; distributed by Del Maguey
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pernod Ricard USA Inc.
FDA (openFDA food enforcement)
Reported May 31, 2023
Incisive CT- whole-body computed tomography (CT) X-Ray System Model Number: 728144
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Headquarters Cambridge
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 31, 2023
truCONTROL 60 Count
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TruVision Health LLC
11 more products in this recall
FDA (openFDA food enforcement)
Reported May 24, 2023
Beckman Coulter Bicarbonate, REF: OSR6137, 4x25 mL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 24, 2023
Mighty Sesame 10.9 Oz Organic Tahini (Squeezable) bottle, UPC 858313006208, 8 Units per case.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kenover Marketing Corp.
FDA (openFDA food enforcement)
Reported May 24, 2023
Distributed by Lipari Foods Ground Cumin in 6oz plastic tub, UPC 094776212620, 12 retail units per wholesale case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods Operating Company, LLC.
FDA (openFDA food enforcement)
Reported May 24, 2023
Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
4 more products in this recall
FDA (openFDA device enforcement)
Reported May 17, 2023
Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported May 17, 2023
BioPlex 2200 REF 665-2050, APLS IgM Pack, APLS IgM Reagent Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported May 17, 2023
Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZB Importing LLC
FDA (openFDA food enforcement)
Reported May 10, 2023
Ultraview SL (UVSL) Command Module, Model 91496
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
FDA (openFDA device enforcement)
Reported May 10, 2023
SafeLight Fiber Optic Cable: Clear, 5MM X 10FT 3.05M, REF: 0233-050-100; Gray, 5MM X 10FT 3.05M, REF: 0233-050-200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported May 3, 2023
(1) Carefusion V. Mueller Graves Vaginal Speculum, Catalog #GL11, Medium Blade, 4 x 1 3/8" (10.2 X 3.5cm); and (2)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
FDA (openFDA device enforcement)
Reported May 3, 2023
FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 828.051
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard Wolf GmbH
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 26, 2023
FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems, REF: RFIT-ASY-0116, (30 pouches/kit)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Apr 26, 2023
Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien
FDA (openFDA device enforcement)
Reported Apr 26, 2023
AQURE REF 933-599 Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 The AQURE system is intended to let you manage…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Step Bladeless Trocars, 10 mm cannula and dilator with radially expandable sleeve and 5 - 10 mm reducer, Product Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Edward Lifesciences, REF 777F8, Swan-Ganz CCOmbo V, CCO/SvO2/CEDV/VIP, Thermodilution Catheter, Exterior Diameter 8F…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Outset Tablo Model Numbers (REF): PN-0006000 PN-0007001 Tablo is a next generation, self-contained hemodialysis system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Outset Medical, Inc.
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Frozen Organic Strawberries, Kirkland Signature, frozen, net wt. 4lb., 9 packages per case, Costco Item 904984. UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Scenic Fruit Company, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 12, 2023
Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath, 8.5F(Small), REF D-1385-01-S, RX CE 2797, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster, 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.