All recall categories

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.

Food

Reported Jun 14, 2023

Chili Cacahuate Japones, net weight 5 oz (127g), packaged in a soft teal colored plastic pouch with the UPC code 7…

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

Werner Gourmet Meat Snacks, Inc.

FDA (openFDA food enforcement)

Food

Reported Jun 7, 2023

Black Fungus Golden Koi 2.5 oz packages 100 bags per case UPC: 81005681145 Product of China

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

AH USA Group Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 7, 2023

Elekta Medical Linear Accelerator (ELMA) included in the below platforms: a. Elekta Infinity; b. Versa HD; c. Elekta…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Food

Reported May 31, 2023

Backpacker s Pantry Blueberry Peach Crisp, 4.6-ounce, packaged in a pouch, UPC-048143026143

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

American Outdoor Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 31, 2023

Incisive CT- whole-body computed tomography (CT) X-Ray System Model Number: 728144

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

Philips Headquarters Cambridge

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 31, 2023

truCONTROL 60 Count

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

TruVision Health LLC

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 24, 2023

Beckman Coulter Bicarbonate, REF: OSR6137, 4x25 mL

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

Beckman Coulter Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 24, 2023

Distributed by Lipari Foods Ground Cumin in 6oz plastic tub, UPC 094776212620, 12 retail units per wholesale case

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

Lipari Foods Operating Company, LLC.

FDA (openFDA food enforcement)

Medical devices

Reported May 17, 2023

Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2023

BioPlex 2200 REF 665-2050, APLS IgM Pack, APLS IgM Reagent Pack

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

Bio-Rad Laboratories, Inc.

FDA (openFDA device enforcement)

Food

Reported May 17, 2023

Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case

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

ZB Importing LLC

FDA (openFDA food enforcement)

Medical devices

Reported May 10, 2023

Ultraview SL (UVSL) Command Module, Model 91496

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

Spacelabs Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 10, 2023

SafeLight Fiber Optic Cable: Clear, 5MM X 10FT 3.05M, REF: 0233-050-100; Gray, 5MM X 10FT 3.05M, REF: 0233-050-200

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

Stryker Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 26, 2023

FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems, REF: RFIT-ASY-0116, (30 pouches/kit)

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 26, 2023

Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner…

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

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Apr 26, 2023

AQURE REF 933-599 Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 The AQURE system is intended to let you manage…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2023

Edward Lifesciences, REF 777F8, Swan-Ganz CCOmbo V, CCO/SvO2/CEDV/VIP, Thermodilution Catheter, Exterior Diameter 8F…

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

Edwards Lifesciences, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 19, 2023

Kagome Worcester Sauce 6/60 fl oz. Ingredients: Water, Sugar, Salt, Fermented Vinegar, Glucose, Tomato Extract, Caramel…

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

Mutual Trading Company Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 19, 2023

Outset Tablo Model Numbers (REF): PN-0006000 PN-0007001 Tablo is a next generation, self-contained hemodialysis system…

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

Outset Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 12, 2023

Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath, 8.5F(Small), REF D-1385-01-S, RX CE 2797, Sterile

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

Biosense Webster, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 12, 2023

Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

COVIDIEN Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed REF 86051 7.0 mm I.D. The Shiley Lo-Pro Oral/Nasal Tracheal Tube…

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

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

Instructions for Use for the following Leksell Stereotactic System and Leksell Neurosurgical Instruments: (1) Part…

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

Elekta Instrument AB

FDA (openFDA device enforcement)

Medical devices

Reported Apr 5, 2023

Irvine Scientific Oil for Embryo Culture (Light Mineral Oil) REF Catalog # 9305

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

Fujifilm Irvine Scientific, Inc.

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.