All recall categories

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.

Medical devices

Reported Dec 27, 2023

0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL: 10ML FILL SYRINGE/9210; NURSE ASSIST: 3ML IV…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Nurse Assist, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

AirFit N10 Nasal Masks and User Guide

High riskUsing this product could cause serious injury, illness or death — stop using it now.

ResMed Ltd.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 20, 2023

Sienna Bakery Chocolate Decadent Brownies (Tray)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dianne's Fine Desserts

FDA (openFDA food enforcement)

Food

Reported Dec 20, 2023

Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe Cookie, Cake and Brownie Collection

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Houdini Inc.

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 20, 2023

CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP)…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 20, 2023

Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX REF 420-159 Spectranetics Turbo-Elite Laser Atherectomy…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 13, 2023

Whole cantaloupe 3ct and 6ct

High riskUsing this product could cause serious injury, illness or death — stop using it now.

FreshPoint Dallas

FDA (openFDA food enforcement)

Medical devices

Reported Dec 13, 2023

Freedom Boom models series: F110, F120, F130, F320, F330, F350, F410, and F420 with built in 42A Lightweight Spring Arm…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ihb Operations B.v.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

RANDOX Total Bilirubin.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Randox Laboratories Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

EVO+VISIAN Implantable Collamer Lens, REF:VICM5_12.1. Phakic Intraocular lens.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Staar Surgical Company

10 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 13, 2023

Vermont Village Organic Unsweetened Apple Sauce (24oz); UPC 362401 | 084648311285

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 6, 2023

Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Edwards Lifesciences, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 6, 2023

Chickpea Veggie Crisps, Net Wt. 6 1/4 oz (177.1g), UPC: 02840020646

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Frito-Lay, Inc. Headquarters

FDA (openFDA food enforcement)

Medical devices

Reported Nov 29, 2023

BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

Ventlab, LLC AirFlow manual resuscitator devices with integrated manometer, multiple accessory configurations to…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

SunMed Holdings, LLC

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 22, 2023

AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Biomedical Division

FDA (openFDA device enforcement)

Medical devices

Reported Nov 22, 2023

IBA Proton Therapy System - PROTEUS 235. PTS-11 versions, PTS-12 versions with Orion PPS version OSS6.0. Configured…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ion Beam Applications S.A.

FDA (openFDA device enforcement)

Food

Reported Nov 22, 2023

Guilt Free No Sugar Added Ice Cream Homemade Vanilla 1.5qts

High riskUsing this product could cause serious injury, illness or death — stop using it now.

TH Searcy LLC

FDA (openFDA food enforcement)

Food

Reported Nov 15, 2023

Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

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.