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.

2,592 stored notices name Arkansas, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.

Food

Reported Mar 23, 2022

Honey BBQ Snack, NO MSG Seasoning packaged in the following sizes: 1. 685-A, Net Wt 21 lbs. (9.52kg). Part #020001456.…

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

PS Seasoning & Spices, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 23, 2022

Fresh Creative Foods THAI PEANUT DRESSING R&G 80/2.5 OZ UPC: 10013454378387 Item # 402464 Perishable/Keep refrigerated

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

RMJV, LP dba Fresh Creative Foods

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 16, 2022

ExacTrac Dynamic software model numbers: 20910-01, ETD Positioning and Moni. 1.0.0 INST; 20910-01A, ETD Positioning and…

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

Brainlab AG

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2022

CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex

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

Carl Zeiss Meditec, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 16, 2022

Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single serve meal to end consumer

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

Factor

FDA (openFDA food enforcement)

Food

Reported Mar 16, 2022

La Fiesta brand, Salted Plums with Chili Product. Product is packaged in cello bags, net wt. 1oz. UPC 0 32327 02829 0.…

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

la fiesta food products

FDA (openFDA food enforcement)

Medical devices

Reported Mar 16, 2022

1688 Camera Control Unit (CCU), Catalog number:1688010000. Used in general laparoscopy, nasopharyngoscopy, ear…

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

Stryker Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2022

Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift

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

Acorn Stairlifts, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2022

AU/DxC AU Magnesium, Catalog/REF Number OSR6189, UDI 15099590010850

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Drugs

Reported Mar 9, 2022

All Over-The-Counter (OTC) drug products sold by Family Dollar retail stores located in Alabama, Arkansas, Louisiana,…

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

Dollar Tree Distribution, Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Mar 9, 2022

da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2022

OPAQUE Herrick Lacrimal Plugs, HP3, 0.3 mm, HP5, 0.5mm, HP7, 0.7.mm, STERILE, EO, Rx only, CE Dry eye treatment

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

Lacrimedics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2022

NavitrackER Kit A: Knee, Model Number 20-8000-000-07,

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

Orthosoft, Inc. dba Zimmer CAS

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2022

Philips Respironics V60 Ventilator Part Number 1053617

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

Respironics California, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 2, 2022

Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF…

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

Medtronic Vascular, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 2, 2022

NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R

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

Nobel Biocare USA LLC

FDA (openFDA device enforcement)

Food

Reported Feb 16, 2022

Amy's Vegan Organic Rice Mac & Cheese; frozen; 8 oz. (227 g) individually packaged serving; in trays with plastic…

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

Amys Kitchen Inc.

FDA (openFDA food enforcement)

Food

Reported Feb 16, 2022

Wishbone Thousand Island Dressing 15oz. bottle UPC 0-41321-00645-6 and 24 oz. bottle UPC 0-41321-00731-6; six bottles…

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

Conagra Brands

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 9, 2022

CRYPTOCOCCAL ANTIGEN LATERAL FLOW ASSAY, IMMY, Lateral Flow Assay for the Detection of Cryptococcal Antigen in serum…

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

Immuno-Mycologics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 9, 2022

Vagus Nerve Stimulation (VNS) Therapy Leads, PerenniaDURA, Model: 303. Model 303-20 PereniaDURA Lead (2.0 mm electrode…

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

LivaNova USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 9, 2022

ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 2, 2022

Brownie Points Schmurtle 2oz Packaged in food grade cellophane only used as gift basket filler - not sold individually

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

Brownie Points LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 2, 2022

GE Vscan Extend, being sold as "Vscan Extend Console"

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

GE Healthcare, LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 2, 2022

Trilogy Evo, Material Numbers DS2110X11B (USA) and KR2110X15B (Korea) The Trilogy Evo ventilator provides continuous or…

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

Philips Respironics, 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.