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 May 4, 2016
3M Steri-Vac Gas Sterilizer/Aerator, models 5XL and 8XL.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported May 4, 2016
Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar Cat. Number 221291, Lot Number 6034889, Exp.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported May 4, 2016
Trinity Acetabular System Product Usage - Total Hip Replacement.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Corin USA Limited
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 4, 2016
Radionuclide Radiation Therapy System Product The product is a teletherapy device intended for stereotactic irradiation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2016
Family Gourmet Long Grain Enriched White Rice, 32 oz. (2 lb.) plastic bag (SKU: 1218898)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Family Dollar Stores - NC Distribution Center
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 4, 2016
GE Healthcare, Aisys and Aisys CS2. Intended to provide general inhalation anesthesia and ventilator support to a wide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
FDA (openFDA device enforcement)
Reported May 4, 2016
CF InPlex ASR Card; Catalog Number: 95-0501.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 4, 2016
ABX Pentra 400 (version 5.0.8 or lower) The ABX PENTRA 400 and 400C are discrete photometric bench top chemistry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Horiba Instruments Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 4, 2016
EndoWrist Stapler 45 and Stapler 30 instruments used on the da Vinci Xi systems (IS4000) with p5 software. General…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2016
RESTORIS PST RIO Offset Shell Impactor For use by orthopedic surgeons specifically for the purpose of positioning and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported May 4, 2016
Andrographis extract 400 mg packaged in a white and orange bottle containing 90 capsules. The bottle has a blue cap and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NOW Foods
4 more products in this recall
FDA (openFDA food enforcement)
Reported May 4, 2016
Suan's Scotch Bonnet Pepper Relish 9.8 oz. packaged in a glass jar with a metal lid.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.S & S Foods, Inc.
FDA (openFDA food enforcement)
Reported May 4, 2016
Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported May 4, 2016
The Super Elixir By WelleCo Australia Alkalising Greens 150g/5.3 oz net, 300g/10.6 oz net Fine Powder welleco.com
High riskUsing this product could cause serious injury, illness or death — stop using it now.Welle Pty Ltd.
FDA (openFDA food enforcement)
Reported Apr 27, 2016
Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit; Catalog number M4U534L; For In Vitro Use…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Biocare Medical, LLC
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Self-Cath¿ Pediatric Catheter Size CH 06, Product # 5044101400, Catakig # 306. Product Usage: The Self-Cath…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coloplast Manufacturing US, LLC
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Starbuck's Cheese & Fruit Bistro Box NET WT 5.3 OZ/150g packaged in non-flexible plastic container.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flying Foods LLC
FDA (openFDA food enforcement)
Reported Apr 27, 2016
Leica Microsystems (Schweiz) Ag. The common name of the device is surgical microscope. It has been assigned the product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2016
GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, 6 x12, 1 x 18, 1 x 48, 1 x100, 36 x 4, Mighty Mango Fruit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Materne North America Corp.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 27, 2016
MEVION S250 for Proton Radiation Therapy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mevion Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2016
GERBER Organic 2ND FOODS Pears, Carrots & Peas, 3.5 oz., film pouches, 6 pouches per display box/ 2 display boxes per…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle Infant Nutrition
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 27, 2016
iVue and iVue 500 (now called iScan) OCT systems with software version 2016.0.0.127 (USA only) and 2016.1.0.127 (out of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Optovue, Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Siemens SOMATOM Definition: Intended to produce cross-sectional images of the body. Computed tomography (CT) x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
The Concerto Basic Shower Trolley is intended for assisted hygiene care, especially showering and bathing of residents…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arjo, Inc. dba ArjoHuntleigh
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.