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 48,122 notices were distributed nationwide, so they reach Oklahoma too — those are in the archive.
Reported Sep 21, 2016
1. Roasted & Salted Sunflower Kernel, 0.7 oz plastic bag, Distributed by Newport Ingredients, Los Angeles, CA 90036; 2.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.SunOpta Food and Grain, Inc.
15 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 20, 2016
Speedy Foods Retira Del Mercado Productos De Rollitos De Primavera De Pollo (“Spring Rolls”) Debido A Un…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Speedy Foods LLC
USDA FSIS
Reported Sep 14, 2016
NOMAD Pro Packaged X-Ray System, Part Number 08500009; NOMAD Pro Vet Packaged X-Ray System, Part Number 08500011; NOMAD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aribex Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 14, 2016
Medical Linear Accelerator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 14, 2016
Affinity Four Birthing Bed Model P3700 The primary packaging is pictured below, and utilizes a metal packing brace,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Sep 14, 2016
The system provides the ability to transmit patient data files for storage, viewing and analysis at distributed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Sep 14, 2016
WECK¿ Horizon" Manual-Load Ligating Clip Applier, For Medium-Large Size Horizon Ligation Clips Curved Jaw, 11 (28cm),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Sep 14, 2016
Activia FIBER Lowfat Yogurt Strawberry/Pineapple Flavors 12 Packs of 4 OZ Cups UPC 3663202884 packaged in form fill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Dannon Company, Inc.
FDA (openFDA food enforcement)
Reported Sep 7, 2016
Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Vision Ab
FDA (openFDA device enforcement)
Reported Sep 7, 2016
RadSuite software. The firm name on the label is Merge Healthcare, Hartland, WI. RadSuite provides a means to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 7, 2016
A7 Anesthesia Delivery System, a device used to administer to a patient, continuously or intermittently, a general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Sep 7, 2016
SPECULAR MICROSCOPE CEM-530; Software version 1.08 and 1.09. Opthalmic: The NIDEK Specular Microscope CEM-530 provides…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Sep 7, 2016
Tippins 8" Key Lime Pie packaged in aluminum pie plates with plastic covers. The responsible firm listed on the label…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tippin's Gourmet Pies, LLC
4 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 7, 2016
Primo Fresh Serrano Peppers Distributed by Warren Produce, 824 W. Monte Cristo Rd, Edinburg, TX packaged in 1/4 bushel…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Warren Produce Co., LLC
FDA (openFDA food enforcement)
Reported Aug 31, 2016
Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.05m) Cable, Catalog Number 51-7310.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Conmed Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Large QWIX Compression screw, dia. 7.5 mm L 90 mm, Lot No. FH86, Rx only, Product Usage: The QWIX Positioning screw is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Medtronic, Viva Quadripolar Implantable Cardioverter Defibrillators: Product Model VIVAXTCRT-D DTBA1D1, DTBA1D4…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
RadSuite software. The firm name on the label is Merge Healthcare, Hartland, WI.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics. Product Usage: RADIESSE is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography X-ray systems intended to produce…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Xpert MRSA Catalog GXMRSA-120, Rev. AJ Microbiology: The Cepheid Xpert MRSA assay performed in the GeneXpert Dx System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cepheid
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Summer Vegetable Salad with Seared Chicken, Garlic Croutons, and Mustard-Chive Vinaigrette
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hellofresh
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 24, 2016
Hospira RECEPTAL CANISTERS: 1L(1000mL), 1.5L(1500mL), 2L(2000mL) Canister, ATS, 2000, with Valve 1) List Numbers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2016
Golden Dipt¿ Jalape¿o Breader is in a white 10 pound bag with the UPC number 763089721548 and Item Number: G5620.690.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerry, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Free recall alerts
Get alerted about new Oklahoma recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
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.