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. A further 48,784 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.

Medical devices

Reported Oct 28, 2020

BD Nexiva Closed IV Catheter System Dual Port (20 GA 1.75 IN) Catalog (Ref) No. 383538 BD Nexiva closed IV catheter…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic…

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen FIA is a lateral flow immunofluorescent sandwich assay…

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

Quidel Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). Procedure Pack REF:…

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Food

Reported Oct 28, 2020

Marketside brand Cranberry Walnut Salad in 4.5 oz. plastic bowl with poly film lidding (6 bowls per case). UPC:…

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

Taylor Farms Tennessee, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 28, 2020

Langston Dual Lumen Catheter

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

Vascular Solutions, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 28, 2020

Shirakiku brand Black Fungus (Kikurage); 5 lb. bag, 6 x 5 lb. bags per case Item # 60403; UPC 0 74410 60403 5…

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

Wismettac Asian Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 21, 2020

Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health" PROTEXIS" Latex Micro Surgical Gloves - Product…

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

Alcon Research, LLC

FDA (openFDA device enforcement)

Food

Reported Oct 21, 2020

Watermelon 10 oz UPC Code: 681131180672; Watermelon 32 oz UPC Code: 681131180689; Watermelon Chunks 42 oz UPC Code:…

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

Country Fresh Inc.

15 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 21, 2020

Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI -…

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

Mizuho OSI

FDA (openFDA device enforcement)

Medical devices

Reported Oct 14, 2020

MICROFLEX Diamond Grip Examination Gloves, MF-300 - Product Usage: A patient examination glove is a disposable device…

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

Ansell Healthcare Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 14, 2020

Bard Conquest PTA Balloon dilation Catheter, 6mm x 40mm, 75 cm, Cat. No. CQ7564, UDI: (01) 00801741062902 - Product…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 14, 2020

DJO EMPOWR Tibial Knee Punch Handle Part No. 801-05-040 and 801-05-018 contained in Instrument Tray for EMPOWR Porous…

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

Encore Medical, LP

FDA (openFDA device enforcement)

Food

Reported Oct 14, 2020

SKIPPY Super Chunk Peanut Butter 16.3oz UPC: 00037600110723 packaged in non-flexible plastic container

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

Hormel Foods Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Oct 14, 2020

PermaFlo Flowable Composite REF-UP 948 Shade: A2 - Product Usage: is a light cured, radiopaque, methacrylate based,…

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2020

Pacific Xtreme (PTCA Balloon Dilation Catheter)

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

ev3 Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2020

Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 18 mm.

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

Exactech, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Oct 7, 2020

Metformin Hydrochloride Tablets USP, 1000 mg, 60-count bottles, Rx Only, Manufactured for: Heritage Pharmaceuticals…

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

Legacy Pharmaceutical Packaging LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Oct 7, 2020

Control, Calibrator Verified, Triage BNP, Model ALR88755

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2020

Speed Stitch Needle Cassette

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

ArthroCare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2020

NM/CT 850 Model Number: H3907AD

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

GE Healthcare, LLC

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 23, 2020

Spicy Beef & Vegetables with Rice & Sesame Seeds meal kits containing onions delivered the week of July 27, 2020.

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

Blue Apron Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 23, 2020

Red Onions, Bulk

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

Lancaster Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2020

The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive Software v1.2 for 7500 RTPCR…

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

Life Technologies Corporation

1 more product in this recall

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.