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 Apr 19, 2017
VIDAS Estradiol II, Ref 30431-01, 60 tests The VIDAS Estradiol II (E2 II) assay is intended for use on the instruments…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Apr 19, 2017
LIDIA'S MARINARA, NET WT 25 oz (708g), UPC 897712001018 --- Manufactured for Nonna Foods LLC Woodbury, NY 11797
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nonna Foods
FDA (openFDA food enforcement)
Reported Apr 19, 2017
Specimen Gate Laboratory; Product Number: 5002-0180 Specimen Gate Laboratory is intended for use as a data processing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PerkinElmer Life and Analytical Sciences, Wallac, OY
FDA (openFDA device enforcement)
Reported Apr 19, 2017
Radiation Therapy Treatment Planning System, Model 4.5, 4.7, 5.0 RayStation is a software system designed for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Apr 19, 2017
CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Apr 12, 2017
DX-D600 - DXD Imaging Package
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Apr 8, 2017
Mibo Fresh Food Recalls Turkey Salad Products Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.MIBO Fresh Foods LLC
USDA FSIS
Reported Apr 5, 2017
AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for use in providing diagnostic quality images to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Apr 5, 2017
JResultNet drivers using ASTM coding language. Calculator/data processing module, for clinical use - Stand-alone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Data Innovations, LLC
FDA (openFDA device enforcement)
Reported Apr 5, 2017
The product is packaged in a white plastic bottle with green lettering. The label reads in part "LIFE RISING DHZC-2,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Life Rising Corp. S
FDA (openFDA food enforcement)
Reported Apr 5, 2017
Great Midwest Applewood Smoked Gouda Cheese, approximately 6 lbs, keep refrigerated
High riskUsing this product could cause serious injury, illness or death — stop using it now.Saputo Cheese USA, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 29, 2017
Mammotome Revolve Dual Vacuum Assist Biopsy System The device is used to sample breast tissue that has been identified…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Devicor Medical Products Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Strawberry Gelato, 5 Liter, 1 unit/case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dolce Dolci LLC dba Villa Dolce Gelato
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 29, 2017
Hitachi Oasis MRI System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Merge Cardio software using EchoIMS. The firm name on the label is Merge Healthcare, Hartland, WI.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Raindrop Near Vision Inlay, Model# RD1-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Revision Optics Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2017
Sargento Ultra Thin Sliced Longhorn Colby, 6.84 oz., UPC 4610000228, with Sell By dates of 12APR17B, 02FEB17F,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sargento Foods, Inc.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 29, 2017
Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Mar 22, 2017
BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 22, 2017
Bivona¿ TTS (Tight to Shaft) Pediatric Tracheostomy Tube, Model No. 67SP035, Reorder No. 67SP035.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Mar 22, 2017
Terumo Advanced Perfusion System 1-Level Sensor II Pads, Product Usage: Ultrasonic couplant used to facilitate the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 22, 2017
Toshiba Kalare DREX-KL80 X-ray generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Great Shake Fortified Nutrition, Soy Formula, Chocolate Artificially Flavored, Packaged in 4 fl oz. (118 mL), and 6 fl…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hormel Foods Corporation
5 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 15, 2017
Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
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.