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 Feb 27, 2013
Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Animas Corporation
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Feb 27, 2013
MAYFIELD¿ Composite Series Base Unit Standard, Model (A3101), Rx ONLY, Integra LifeScience Corporation, 4900 Charlemar…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Lean Cuisine Culinary Collection Mushroom Mezzaluna Ravioli ravioli filled with portobello & button mushrooms, romano &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle USA
FDA (openFDA food enforcement)
Reported Feb 27, 2013
Vascular Solutions, SuperCross Microcatheter, Sterilized using ethylene oxide, Rx Only, Model numbers 5300 - 5307,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Feb 20, 2013
The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for use under direct or endoscopic visualization for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lumenis Limited
FDA (openFDA device enforcement)
Reported Feb 20, 2013
Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mizuho OSI
FDA (openFDA device enforcement)
Reported Feb 20, 2013
St. Jude Medical, AGA Medical corporation, AMPLATZER¿ TorqVue¿ FX Delivery System. Model #'s: 9-ITVFX06F45/60,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.St Jude Medical Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Diagnostic Hybrids Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Li-Ion battery used in the Oxus Portable Oxygen Concentrator (POC), RS-00400. Also branded as Reliability Plus byDrive.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oxus America, Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion - 2.5mm Drill Bit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 13, 2013
PREMIER LIFECARE RECLINER 5400 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012 A multi position…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Winco Mfg., LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Cordis, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device, cat. No EX500, EX600, and EX700. Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Esteem Programmer Model 6001, US and ISA, Model 3001 Dell E54XX, part of the Esteem Totally Implantable Hearing System.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Envoy Medical Corporation
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated for bipolar coagulation and mechanical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Spice Cake Mix , 25 lb. and 50 lb. kraft bags, labelled a) CMC Quality and Value, Spice Cake Mix, 46702-00985, NET Wt.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jiffy Food Service, LLC
FDA (openFDA food enforcement)
Reported Jan 30, 2013
Roche COBAS INTEGRA 400 and 400 plus Analyzer, an in vitro diagnostic analyzer.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Jan 23, 2013
Sarns flexible arterial cannula, 6.7 mm (20Fr) OD with 3/8 in. connector, suture ring, 9.5 in (24 cm) long The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 23, 2013
Woodstock All Natural Tamari Almonds, 7.5 OZ in a gusseted re-sealable poly bag.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Woodstock Farms
FDA (openFDA food enforcement)
Reported Jan 16, 2013
Product labeled in part: ***PARAMOUNT RESERVE***PRODUCT OF CHILE FARM RAISED ATLANTIC SALMON PACKED BY: ALIMENTOS…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Multiexport Foods, Inc.
FDA (openFDA food enforcement)
Reported Jan 9, 2013
Fresh Express brand, Fresh Spinach, 9 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Express Incorporated
FDA (openFDA food enforcement)
Reported Jan 9, 2013
Analyzing system consists of a small and portable analyzer and plastic microcuvettes. The microcuvette contains…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.HemoCue AB
FDA (openFDA device enforcement)
Reported Jan 9, 2013
Liko Standard Slingbar 450. The Standard Slingbar 450 is a versatile sling bar which can be used for most lifting…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Jan 9, 2013
ABX PENTRA AST CP, Part Number: A11A01629. The ABX Pentra AST CP reagent is a diagnostic reagent for quantitative in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Horiba Instruments, Inc. dba Horiba Medical
1 more product in this recall
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.