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 Feb 8, 2017
MEVION S250-Proton Radiation Therapy Product Usage: Proton Radiation Therapy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mevion Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2017
Olympus Scientific Solutions Americas Corporation ( OSSA ) VANTA¿ XRF Analyzer. Model Vanta VCR and Vanta VMR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Scientific Solutions Americas
FDA (openFDA device enforcement)
Reported Feb 8, 2017
Jon Donaire Ice Cream Layer Cake, Deliciously moist white cake with rich, creamy strawberries & cream ice cream, NET WT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rich Products Corp.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 1, 2017
FRONT: Stauffer's Animal Crackers Original; Net Wt. 32 OZ.; BACK: (best by date): 07SEP17; (bag lot numbers) LC120716…
High riskUsing this product could cause serious injury, illness or death — stop using it now.D. F. Stauffer Biscuit Co., Inc.
FDA (openFDA food enforcement)
Reported Feb 1, 2017
Hitachi Oasis MRI System - C-Spine Coil
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2017
SCC Soft Computer Softbank II software Product Usage: Supports single and multi-site transfusion services in healthcare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Soft Computer Consultants, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2017
NO EGG CHOCOLATE CHIP COOKIE DOUGH 03-3014, Net Weight 30 lb (13.61 Kg) Aspen Hills, Inc. Garner, IA 50438
High riskUsing this product could cause serious injury, illness or death — stop using it now.Aspen Hills, Inc.
18 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 25, 2017
Novation Cemented Plus Femoral Stem, 12/14, Collared, Standard Offset, Matte, Cemented, Size 15.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2017
PREMIER EHEC and PREMIER EHEC Bulk.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Texas Kitchen Salads Tropical Fruit Supreme KEEP REFRIGERATED Nutrition Facts NET WT. 16 oz. in plastic containers,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ron's Home Style Foods, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2017
Femoral and Tibial Cutting Block Adapter Base. Brainlab knee, BrainLAB Image Guided Surgery System / Instrument,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Jan 18, 2017
In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brand Castle LLC
FDA (openFDA food enforcement)
Reported Jan 18, 2017
Cardboard sleeve: Double Takes Macaroni & Cheese Dinner, Distributed By: Greenbrier International, Inc., 500 Volvo…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fourth Street Barbeque, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2017
OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2017
Innova 2000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2017
SOMATOM Scope, Computed tomography x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
CyberKnife Robotic Radiosurgery Systems, models: G3, G4, VSI. Radiology: The CyberKnife Robotic Radiosurgery System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accuray Incorporated
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Zeus-P Lumbar Interbody Device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amendia, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM SS/SS…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Angiodynamics, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Fresh Express Kit Caesar salad, Net Wt. 7.6 oz. (215g), Fresh Express Incorporated, 550 S. Caldwell St. Charlotte, NC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresh Express Incorpated
FDA (openFDA food 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.