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 15, 2014
saba; ACE; Appetite Control Energy; 052234; 07/2015; Distributed by Saba; 711 NE 39th Street, Oklahoma City, OK 73105
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AMS Health Sciences
FDA (openFDA food enforcement)
Reported Oct 15, 2014
Hostess Frosted Bagged Donettes, 11.25 oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hostess Brands LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 15, 2014
Mars Chocolate North America Milk Chocolate M & M's Net Wt. 3.40 oz packed in a brown, 3 inch x 6.5 inch cardboard box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mars Chocolate North America
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 15, 2014
McKesson Cardiology" Hemo intended for complete physiological/hemodynamic monitoring, clinical data acquisition,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Information Solutions LLC
FDA (openFDA device enforcement)
Reported Oct 15, 2014
Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nemschoff Chairs, Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2014
Mini Butter Croissant 6 Pack Ingredients: Wheat Flour (unbleached enriched wheat flour, malted barley flour, niacin,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market Brand 365, LLC
FDA (openFDA food enforcement)
Reported Oct 8, 2014
Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumed International, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2014
Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
CareFusion AirLife Heated Infant Breathing Circuit Product Usage: Respiratory breathing circuits are used with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
0.9% Sodium Chloride Injection, USP BD PosiFlush(TM) SF Saline Flush Syringe 10 mL REF#306553 used in Centurion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centurion Medical Products Corporation
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instratek, Incorporated
FDA (openFDA device enforcement)
Reported Oct 1, 2014
Spacelabs Medical Patient Monitor is a Physiological, Patient monitor With Arrhythmia Detection or Alarms. The Models…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Oct 1, 2014
EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vidacare Corporation
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 24, 2014
BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen Agar is used to test enterococci for resistance…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Sep 24, 2014
ProVue Instrument Driver for JResultNet (ProVue.jrm) v. 1.5.3 and below JResultNet is a stand-alone software package…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Data Innovations, LLC
FDA (openFDA device enforcement)
Reported Sep 24, 2014
BD Vacutainer Serum Tubes (RED TOP PLAIN TUBE 6.0 ML)Part Number: BD 367815 FMC Part Number: 87-7815-4 Single use tube…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GF Health Products, Inc./d.b.a.Basic American Metal Products
FDA (openFDA device enforcement)
Reported Sep 24, 2014
AXIOM Luminos dRF system with SW VD10 or on Luminos dRF Max The Axiom Luminos dRF is intended to be used as a universal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 24, 2014
Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net wt 1 lb (454 grams), in round 1000 cc High…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Swanson Health Products, Inc.
FDA (openFDA food enforcement)
Reported Sep 17, 2014
AB SCIEX API 3200MD" LC/MS/MS System with software: MultiQuantMD 3.0In vitro diagnostic to identify inorganic or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ab Sciex
FDA (openFDA device enforcement)
Reported Sep 17, 2014
The BD MAX MRSA Assay, catalogue #442953. An automated qualitative in vitro diagnostic test for the direct detection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Sep 17, 2014
PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model PRR35), PROXIMATE PX Fixed-Head Skin Stapler…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Sep 17, 2014
Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Force
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.