Recalls distributed in Oklahoma
These notices name Oklahoma 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.
2,997 stored notices name Oklahoma, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Oklahoma too — those are in the archive.
Reported Dec 13, 2023
Luminex VERIGENE BC-GP Utility Tray (5-Pack Carrier), Gram-Positive Blood Culture Nucleic Acid Test, REF 20-011-018, a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Dec 13, 2023
EVO+VISIAN Implantable Collamer Lens, REF:VICM5_12.1. Phakic Intraocular lens.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Staar Surgical Company
10 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 6, 2023
Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 6, 2023
Chickpea Veggie Crisps, Net Wt. 6 1/4 oz (177.1g), UPC: 02840020646
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Frito-Lay, Inc. Headquarters
FDA (openFDA food enforcement)
Reported Nov 29, 2023
BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Nov 29, 2023
EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Integrity Biochem HSC 70-LM, Alcohol Antiseptic 70%, Hand Sanitizer, Lemon Scented Topical Gel, 208.19 L (55 gallons)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integrity Bio-Chemicals LLC
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 22, 2023
AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Biomedical Division
FDA (openFDA device enforcement)
Reported Nov 22, 2023
Guilt Free No Sugar Added Ice Cream Homemade Vanilla 1.5qts
High riskUsing this product could cause serious injury, illness or death — stop using it now.TH Searcy LLC
FDA (openFDA food enforcement)
Reported Nov 15, 2023
Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA food enforcement)
Reported Nov 15, 2023
BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Breg Inc.
FDA (openFDA device enforcement)
Reported Nov 15, 2023
BD Alaris PCU REF 8015
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 15, 2023
Cordis ANGIOGRAPHIC CATHETERIZATION SETS, INFINITI THRULEMEN, 5F, REF CO0208, cardiac catheter
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cordis US Corp.
FDA (openFDA device enforcement)
Reported Nov 15, 2023
CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT, SKU 900260
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Family Dollar Stores, Llc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 15, 2023
Gills Onions 3 lb. bags, diced yellow onions
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gills Onions, LLC
72 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 15, 2023
StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, with StealthStation…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Nov 15, 2023
Zephyr Endobronchial Valve (EBV) 5.5-LP, REF: EBV-TS-5.5-LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pulmonx, Corp.
FDA (openFDA device enforcement)
Reported Nov 8, 2023
Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular, LLC
FDA (openFDA device enforcement)
Reported Nov 8, 2023
Q2 Multiport Extension set, REF: 9520, Rx Only Sterile, single use non-pyrogenic intravenous fluid administration sets…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quest Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 1, 2023
TruDi Navigation System, Model: FG-2000-00, Catalog: ENS022B, when used with TruDi Curette, Models: TDC0005Z and TDC0005
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acclarent, Inc.
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Betty Lou's Inc.
FDA (openFDA food enforcement)
Reported Nov 1, 2023
Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardinal Health 200, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Astral 100 and Astral 150 ventilators
High riskUsing this product could cause serious injury, illness or death — stop using it now.ResMed Ltd.
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.