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 Aug 19, 2020
Verigene Processor SP with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Tibial knee prosthesis
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Hardware removal kit, Part Number 1985KIT1 - Product Usage: The Wright Medical hardware removal kit is designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wright Medical Technology, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2020
SUTUREFIX ULTRA Suture, Product number 72203855
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2020
Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2020
ClearPro T-Piece Closed Suction Catheter, Model DYNCPTP14, 14 Fr 21.3 IN FOR ENDOTRACHEAL TUBE - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2020
regard Migrating Indicator, STEAM Migrating Indicator Strips, REORDER # 335576REG - Product Usage: The integrating…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Resource Optimization & Innovation LLC
FDA (openFDA device enforcement)
Reported Aug 5, 2020
FSIS Issues Public Health Alert for Ready-to-Eat Meat and Poultry Products Containing FDA-Regulated Onions that have…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Taylor Farms TX, Inc.
USDA FSIS
Reported Aug 5, 2020
Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Ablation Galil Technology, IcePearl 2.0 CX 90 Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Thora-Para 5 Fr Non-Valved Catheter Drainage Tray
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The IPC system is indicated for the incision/cutting removal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2020
BodyGuard BodySet, REF: A120-160SAS
High riskUsing this product could cause serious injury, illness or death — stop using it now.CME America, LLC
36 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2020
This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic devices. NYLATEX WRAP - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Djo, LLC
FDA (openFDA device enforcement)
Reported Jul 22, 2020
Fresh Express Iceberg Garden / Lechuga Repollo 24 oz., UPC 071279104119, iceberg lettuce, carrots & red cabbage
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresh Express Incorporated
91 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 22, 2020
***KIND HEALTHY GRAINS***Oats & Honey Granola with Toasted Coconut***INGREDIENTS: Oats, tapioca syrup, brown rice, cane…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kind LLC
FDA (openFDA food enforcement)
Reported Jul 15, 2020
EasyDiagnost Eleva DRF, model no. 706050 - Product Usage: X-ray system, diagnostic, general-purpose.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2020
Blood gases (PCO2, PO2) and blood pH test system; ABL800 FLEX; Model Number 393-800; UDI (01)05700693938004. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2020
PORT-A-CATH¿ II POWER P.A.C. Low Profile" system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Simply Nature Sweet Potato Bites, 12oz retail boxes variety pack, Expiration date 4/9/2022. Lot code R20AJ-01A.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dr. Praeger's Sensible Foods Inc.
FDA (openFDA food enforcement)
Reported Jul 8, 2020
Sterile Disposable Connectors ASY CONN Y 1/2X1/2X3/8 STR 24. REF/ GTIN for Insert Label:029165000/ 00803622123153
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
21 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mueller Sports Medicine, Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2020
VITROS 3600 Immunodiagnostic System Software Versions 3.3.3 and below Product Code: 6802783, Unique Identifier:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho Clinical Diagnostics
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.