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.

2,595 stored notices name Arkansas, reported between Jun 20, 2012 and Nov 18, 2026.

Medical devices

Reported Mar 11, 2020

Remisol Advance running on hardware with Windows XP, Windows 7, Windows Server 2003 and Windows Server 2008 operating…

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

Normand-Info S.A.S.U.

FDA (openFDA device enforcement)

Food

Reported Mar 11, 2020

Natural Grocers Organic Extra Virgin Coconut Oil, packaged in glass jars with metal lids and a plastic shrink seal,…

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

Vitamin Cottage Natural Food Markets, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 4, 2020

Protective Cover Vivo 55/65 (Used for Vivo 50/65), Part No. 006344. It is an accessory (i.e. protective cover) for the…

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

Breas Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 4, 2020

C&H Pure Cane Sugar Golden Brown, 32 oz (2 LB) plastic bag, UPC 015800090038, Lots 50042 (Best By Jan 21, 2022) & 50043…

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

Domino Foods Inc.

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 4, 2020

Ulrich medical neon3 OCT spinal stabilization, REF CS 3917-12, Locking screw for crosslink, screw-to-screw

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

ulrich medical USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2020

SnapLink, Ref Part No. 438-2190, L6R SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx…

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

Ormco/Sybronendo

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 26, 2020

PS# 58021 Honey BBQ Sauce Sauce (AFP) packed in 9 - 275 gallon totes

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

Pepper Source, Ltd.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 26, 2020

OPTILITE IgM Kit, REF: NK012.OPT.A, IVD, UDI: 05051700017565

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

The Binding Site Group, Ltd.

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2020

Bakers Corner All Purpose Flour in 5 lb. bags

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

Adm Milling

18 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2020

FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B

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

Arrow International Inc.

48 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2020

DaVinci Gourmet, Classic Caramel Flavored Sauce, 128 FL OZ (1 GAL), in plastic jugs

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

Kerry, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2020

Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…

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

Medtronic Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…

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

Pacific Medical Group Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Double-Double, REF 3910-500-472, UDI 07613327464832, Sterile R,…

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

Stryker Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Bulk Pail Product -- Almark Foods HARD COOKED BROKEN EGG WHITES 20 LB pail, DIST BY: ALMARK FOODS, GAINESVILLE, GA…

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

Almark Foods, LLC

28 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205

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

Pacific Medical Group Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

Brasseler USA KM169-39-76 Steinmann Pin Single Diamond Smooth, Diameter 2.8 mm, Length 228 mm Product Usage: A…

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

Brasseler USA I LP

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

GIBSON Healthcare Membrane 6-9, 15mm x 20mm, Reference Number 5303-226 - Product Usage: Indicated for use in oral…

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

Collagen Matrix Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

CS5/5+ Fastpacks, 225 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are…

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

Haemonetics Corporation

21 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2020

Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert

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

Jeni's Splendid Ice Creams LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2020

Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14

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

Johnson & Johnson Surgical Vision Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

AQURE basic sytem, FLEXLINK, REF 933-599, Version: 2.3.3 (17), CE IVD, Rx Only, UDI: (01)05700699335999 Intended use:…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

RayStation stand-alone software treatment planning system. Models 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…

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

Raysearch Laboratories Ab

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.