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.
Reported Feb 14, 2024
Spectral CT on Rails: Software Version 5.1.0.X, model 728334.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Total immunoglobulin M (IgM total) IVD, kit, nephelometry/turbidimetry
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Feb 7, 2024
Rizo Bros Cotija (Grated) 8 oz. UPC 72724200043 7 oz. UPC 7-27242-14022-5 Tio Francisco, Casa Cardenas 9 oz. UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rizo Lopez Foods, Inc. dba Don Francisco Cheese
13 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 31, 2024
PANTHER FUSION System REF 9121010000 The Panther System is an integrated nucleic acid testing system which fully…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Jan 31, 2024
Power Knee, REF: PKA10001, and PKA10003; with Power Knee Battery, REF: PKA10002
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
FDA (openFDA device enforcement)
Reported Jan 31, 2024
Achieva 1.5T, Model No. 781178, 781196, 781296
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Philips North America
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 31, 2024
Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V, REF DWJ001, L: 7mm, Cementless Sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier, Inc.
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Ministry of Snacks Sweet and Savory Collection #8700
High riskUsing this product could cause serious injury, illness or death — stop using it now.Houdini Inc.
FDA (openFDA food enforcement)
Reported Jan 24, 2024
High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123
High riskUsing this product could cause serious injury, illness or death — stop using it now.Percussionaire Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2024
INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phase Scientific International Limited
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Chicken Broth sold under Chef's Cupboard, 32oz Chicken Stock, UPC: 4099100067699, carton Gold Emblem, 32oz Chicken…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TreeHouse Foods, Inc.
14 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 17, 2024
Alinity i Processing Module REF 03R65-01 The Alinity i Processing Module is a fully automated immunoassay analyzer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2024
CD11b APC: ASR, REF: 340936, and CE, REF: 333143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Eban's Bakehouse Sweet Indulgences - Variety Pack (12 pieces/cookies) packaged in 11.85oz cardboard candy box with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eban's Bakehouse LLC
6 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 17, 2024
Incisive CT, model 728143 & 728144 running Software Version 5.0.0.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare (Suzhou) Co., Ltd.
FDA (openFDA device enforcement)
Reported Jan 17, 2024
CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Townsend Design
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 10, 2024
External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 10, 2024
Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Respironics, Inc.
FDA (openFDA device enforcement)
Reported Jan 3, 2024
Alinity ci-series System Control Module, REF: 03R70-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Jan 3, 2024
Sertraline Tablets, USP 100 mg, 30 tablets per bottle, Distributed by: Wal-Mart, Bentonville, AR 72716, Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Legacy Pharmaceutical Packaging LLC
FDA (openFDA drug enforcement)
Reported Dec 27, 2023
Abbott CELL-DYN Ruby, Model CD-Ruby, List number 08H67-01, and Abbott CELL-DYN Sapphire, Model CD Sapphire, list number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Dec 27, 2023
AcuMatch Hip System, Catalog Number 142-32-27
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Injection Needle, REF: 25207
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
4 more products 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.