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 Oct 2, 2019

Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2019

Medfusion¿ Model 4000 Syringe Infusion Pump, with PharmGuard¿ Server Software (PGS). Sold under the following names:…

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

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2019

LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2019

Maquet Cardiopulmonary (MCP)/Getinge HLS Set Advanced 7.0. Model Number BEQ-HLS-7050 USA, Part Number 701052794

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

Maquet Cardiovascular US Sales, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 18, 2019

Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers:…

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

Allergan PLC

14 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2019

YoCrunch VANILLA LOWFAT YOGURT WITH SNICKERS PIECES 4 - 4 oz (113g) - 16 oz (453g) 6 packaged or 4 cups per case. UPC…

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

Danone Waters

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2019

Threaded Offset Cup Impactor - Product Usage: To assist the surgeon in the implantation of Novation hip system…

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

Exactech, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2019

PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g) composite can

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

Natures One Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2019

XP- CR Tibial Tray- Interlok 59mm Item # 195268

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

Zimmer Biomet, Inc.

34 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Norm-O-Temp model 111Z

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

Cincinnati Sub-Zero Products LLC, a Gentherm Company

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2019

EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…

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

Bard Peripheral Vascular Inc.

27 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 4, 2019

PreGel Lemon 50 4.4 lb (2kg) bag, Ingredients: dextrose, citric acid, mono and diglycerides of fatty acids, propane…

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

PreGel America, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 4, 2019

Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System with patient tables as follows: Systems Material…

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

Siemens Medical Solutions USA, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

Kit BD Max Check-Points CPO IVD EU; Catalog # 278102

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

Becton Dickinson & Co.

18 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

ABL90 FLEX Analyzer REF 393090 UDI:05700693930909

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software…

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

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914

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

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 28, 2019

PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 48 oz

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

The Kroger Co.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 21, 2019

Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5…

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

BIMBO Bakeries USA Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 21, 2019

Batter mixes labeled the following ways: 1) Batter, Item Number 30713419.49, Net Wt. 50 lb, Distributed by Kerry…

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

Kerry, Inc.

57 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 14, 2019

The Alinity ci-series System Control Modules which are configured with Alinity c Processing Modules. The Alinity…

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

Abbott GmbH & Co. KG

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2019

Alinity i Ferritin Reagent Kit, List Number 07P6530 The Alinity i Ferritin assay is a chemiluminescent microparticle…

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

Abbott Ireland Diagnostics Division

FDA (openFDA device enforcement)

Food

Reported Aug 14, 2019

Great Value Mild Taco Seasoning, Net Wt. 1 OZ, Distributed by Wal-Mart Stores, Inc. Bentonville, AR. UPC 0 78742 24572v0

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

CH Guenther & Sons, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 14, 2019

IDEAL IMPLANT Structured Breast Implant, saline breast implant, in the following sizes: 210cc, 240cc, 270cc, 300cc,…

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

Ideal Implant Incorporated

FDA (openFDA device enforcement)

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Other states

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.