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 48,132 notices were distributed nationwide, so they reach Oklahoma too — those are in the archive.
Reported Oct 3, 2012
DEXIS Imaging Suite - catalog number 1.008.7932, version numbers 10.0.0 through 10.0.3 Radiological Image Processing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Imaging Sciences International, LLC
FDA (openFDA device enforcement)
Reported Oct 3, 2012
Invacare¿ I-Fit" Shower Chair (Models 9780, 9781, 9781-1), Invacare Corporation, Elyria, OH 44035. These shower chairs…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Oct 3, 2012
Thallous Chloride Tl 201 Injection, Diagnostic Sterile, Non-Pyrogenic Solution, a) 2.8 mL (NDC 0019N12028) b) 6.3ml…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mallinckrodt Inc.
FDA (openFDA drug enforcement)
Reported Oct 3, 2012
SharePlan 1.1, aka t-RayAutoplan version 1.2.1 (build number 1.3.1.10). Manufacturing name RayAutoplan, aka…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Oct 3, 2012
Fruit Mixes: 1) Dining In¿ Super Fruit Medley,10.5oz, UPC 1122508396, Use by date 9/6/2012; 2) Ready Pac¿ Super Fruit…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ready Pac Foods Inc.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 3, 2012
Siemens Magnetom Skyra, Verio, Spectra and Biograph MMR Nuclear Magnetic Resonance Imaging System and Tomographic Imager
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Precise Digital Accelerator Delivery of radiation to defined target volumes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Nitre powder. Brand "Selected Product", 4oz plastic bags, UPC 0 45027 97918 2.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hocean Inc.
FDA (openFDA food enforcement)
Reported Sep 26, 2012
The 2.7mm Drilling Guide is a reusable instrument used in conjunction with a drill to prepare oriented holes in bone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra Life Sci.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Kimberly-Clark MIC Safety PEG Kit - Pull Type The Kimberly-Clark MIC PEG Kits - Pull type are Percutaneous Endoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2012
ProBalance Protein To Go(TM), Milk Chocolate Shake, Dietary Supplement, Net Wt 2.5 fl oz (Responsible firm on labeling:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Protica, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 26, 2012
The product affected by this notice is sold under the trade name TomoTherapy SharePlan 1.1 . To determine if the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Sep 26, 2012
12/14 TAPER HIGH OFFSET NECK USE WITH SMITH & NEPHEW STEMS AND 12/14 FEMORAL COMPONENTS ONLY CO-CR, REF 71352112, Smith…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Spence & Co Ltd brand 8oz Smoked Salmon Trim
High riskUsing this product could cause serious injury, illness or death — stop using it now.Spence & Co., Ltd.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 26, 2012
Infinity¿ sampling device, Cytology Brush, United States Endoscopy Group, Inc., 5976 Heisley Road, Mentor, OH 44060 The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Reported Sep 19, 2012
Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T, ST241T, ST242T, ST243T, ST244T, and ST245T). The S4 Spinal System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
FDA (openFDA device enforcement)
Reported Sep 19, 2012
Sterile Empty Vial and Injector (30mL PCA vial), Rx only, One/List No. 6021-03, Hospira, Inc., Lake Forest, IL 60045.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira, Inc.
FDA (openFDA device enforcement)
Reported Sep 19, 2012
Crown Program BK Fresh Apple Slices, 2 oz On or before August 13; no upc code
High riskUsing this product could cause serious injury, illness or death — stop using it now.Missa Bay, LLC
28 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 19, 2012
Omnilife Science Apex Knee System Modular Tibia Augment, Size 1 x 4mm Ref: KC-54010. The Apex Knee System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Omni Life Science
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2012
Nature's Harvest, pine nuts, Net WT 3 oz (85 g), Distributed by Amport Foods, 550 Kasota Ave, SE., Minneapolis, MN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Importing Co., Inc.
FDA (openFDA food enforcement)
Reported Sep 12, 2012
AmeriWater MRO Dialysis RO+ System, AmeriWater 1303 Stanley Avenue, Dayton, OH 45404 (800) 535-5585 www.AMERIWATER.com.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AmeriWater Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2012
BD GeneOhm MRSA ACP Assay Catalog #441637, box 48 tests labeled in part***GeneOhm Sciences Canada, Inc., 2555 boul, du…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2012
OPTETRAK LOGIC TIBIAL INSERT POSTERIOR STABILIZED***Match Component Colors 6 YELLOW, 11mm, Use with LOGIC Femoral and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2012
VersaTREK Windows Software, Version 5.4.3 is a component of the VersaTrek System. The Software CD will be individually…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Trek Diagnostic Systems
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.