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 Mar 9, 2016
BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2016
(Stryker) AccuPlace Straight Level Needle Guide; Assists the user with inserting a needle at a predetermined angle for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2016
BD FMC7 FITC: Model 430918. FMC7 is intended for in vitro diagnostic use in the identification of cells expressing FMC7…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Mar 2, 2016
Fresenius Naturalyte Liquid Acid Concentrate Catalog Number: 08-2301-3 Intended Use: Acid Concentrate for Bicarbonate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Renal Therapies Group, LLC
FDA (openFDA device enforcement)
Reported Mar 2, 2016
Hill-Rom Bariatric Power Recliner, Product Model # P9096 Hill-Roms 660 lb Powered Bariatric Recliner was created to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2016
This reagent is for in vitro diagnostic use. Pax-5 (1EW) monoclonal antibody is intended to be used for the qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Feb 24, 2016
REF 0038460 Toomey Syringe 70cc Syringe with Catheter Tip and Luer Tip Adapters, Single Use, Rx Only, Latex Free, 50…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Feb 24, 2016
Dark Chocolate, Milk Chocolate, & Yogurt Covered cranberries, Net Wt. 5 oz (140g) Packaged under the following names:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cape Cod Provisions LLC
FDA (openFDA food enforcement)
Reported Feb 24, 2016
fentaNYL Citrate, Preservative Free, 5 mcg per mL In 0.9% Sodium Chloride, 1 mL Total Volume For IV Use, packaged in a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pharmedium Services, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Feb 19, 2016
Flying Food Group, LLC Recalls Ready-To-Eat Wraps Due to Adulteration, Misbranding, and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Flying Food Group, LLC
USDA FSIS
Reported Feb 17, 2016
Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet France SARL
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Arctic Sun 5000 and Arctic Sun 2000; Intended for monitoring and controlling patient temperatures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2016
RadSuite, a picture archive and communications system. Model Numbers Versions 5.30.0, 5.30.1, 5.30.2, 5.30.2 SB0344,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2016
MEVION S250 Radiation therapy system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mevion Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2016
McCain Foods USA, Inc. Recalls Pork Products Due To Possible Foreign Matter Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCain Foods USA, Inc.
USDA FSIS
Reported Feb 10, 2016
API ZYM Bx2 (Ref 70493) Product Usage: ZYM B reagent is an additional test used for revealing the results of some…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Feb 10, 2016
Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080. Volume controlled emergency and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 10, 2016
The ABX PENTRA Cholesterol CP ref. A11A01634 is an in vitro diagnostic assay for quantitative determination of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Horiba Instruments Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 10, 2016
Dove Chocolate Assortment Snowflakes Net. Wt. 24.0 oz. Distributed by Mars Chocolate na, llc Hackettstown, NJ…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mars Chocolate North America
FDA (openFDA food enforcement)
Reported Feb 10, 2016
AQURE System; Model Number: 933-599. The AQURE System manages blood gas and immunoassay analyzers.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Feb 10, 2016
Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-invasive homecare devices, for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Resmed Corporation
FDA (openFDA device enforcement)
Reported Feb 10, 2016
Biosure Driver, Product No: 72201887 For delivery and placement of orthopedic screws. Orthopedic Manual Surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc., Endoscopy Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 10, 2016
This Kid Saves Lives Chocolate Chip UPC #10858497004097 UPC# 858497004090
Moderate riskThis product could cause temporary or reversible health problems — stop using it.This Bar Saves Lives
FDA (openFDA food enforcement)
Reported Feb 3, 2016
Vantage Panoramic X-Ray System used to perform dental and orthodontic radiological imaging The Vantage Panoramic X-Ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Midmark Corp. dba Progeny Inc.
FDA (openFDA device 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.