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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.

Medical devices

Reported Jul 2, 2014

Glucose Hexokinase Liquid Reagent For the in vitro quantitative determination of Glucose in serum.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

JAS Diagnostics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System is intended to provide invasive or…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nellcor Puritan Bennett Inc. (dba Covidien LP)

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray System & Brilliance CT Big Bore Radiology Whole…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Siemens StreamLAB(R) Analytical Workcell; Catalog number 746002.901. Designed to automate sample handling and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Spacelabs Healthcare Qube Compact Monitor, Model 91390. Intended to alert the user to alarm conditions that are…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spacelabs Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

ANSPACH***Knotless Suture Anchor Deployment Tool, Custom***Rx Only*** This device is intended to be used with Anspach…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Anspach Effort, Inc.

44 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Western / Scott Fetzer Company

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

VerSys¿ Hip System, Beaded Fullcoat Stems, Zimmer, Inc., Warsaw, IN 46581

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 25, 2014

liveGfree Gluten Free Blueberry Pancakes NET WT 14.4 OZ, 12 pancakes Keep Frozen Distributed By Aldi, Inc., Batavia, IL…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

American Waffle

FDA (openFDA food enforcement)

Medical devices

Reported Jun 25, 2014

Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a component of the Puritan Bennett 840 Ventilator:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nellcor Puritan Bennett Inc. (dba Covidien LP)

FDA (openFDA device enforcement)

Food

Reported Jun 18, 2014

Poco Pac Salad Dressing, Distributed by Diamond Crystal Brands, Inc., Savannah, GA 31405, and packaged in single serve…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Diamond Crystal Brands, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 18, 2014

RUSCH Easy Cath Coude Kit, 10 FR, Rx Only, Sterile, Distributed by: Teleflex Medical, Research Triangle Park, NC 27708.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teleflex Medical

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 11, 2014

American Spoon¿ Sour Cherry PRESERVES Richer in Fruit (56 Brix) Made in Small Batches Net Wt. 9.5 oz/269g, glass jar…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

American Spoon Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 11, 2014

BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive (BioGlue) is indicated for use as an adjunct to…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CryoLife, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 11, 2014

CARINAsim MAN-1236 Rev 2 and CARINAiso MAN-1237 Rev 2 laser software. LAP isocenter marking control software. Laser…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lap

FDA (openFDA device enforcement)

Food

Reported Jun 11, 2014

Greens+ Vegan Crisp Bars - Dark Chocolate Almond Blueberry in 1.4 oz packages.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Orange Peel Enterprises, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 11, 2014

CAPTAIN KRATOM GOLD XL 30 Grams MAENG DA CAPSULES CAPTAIN KRATOM GOLD 15 GRAMS MAENG DA CAPSULES CAPTAIN KRATOM PREMIUM…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Prep Enterprises LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 11, 2014

AXIOM Luminos dRFsystem The Axiom Luminos dRF is intended to be used as a universal diagnostic imaging system for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 4, 2014

The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare

FDA (openFDA device enforcement)

Food

Reported Jun 4, 2014

Organic traditions DARK CHOCOLATE GOLDEN BERRIES***DAIRY & SUGAR FREE 80% DARK CHOCOLATE; Pack sizes 3.5oz/100g, UPC 8…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Health Matters America Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 4, 2014

Organic Cocoa Cassava bars, 1.59 oz (45 g), individually packaged in foil pouches and sold under the Dr. Mercola brand.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mercola Group

FDA (openFDA food enforcement)

Medical devices

Reported May 28, 2014

GE Healthcare, NeuroMuscular Transmission Module, E-NMT-01 Product Usage: The Datex-Ohmeda S/5TM E-NMT module is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 28, 2014

LATEX-FREE; EXTENSION SET; For Bladder Irrigation or Urinary Drainage, Compatible with T-U-R FLOW-POUCH RESERVOIR, list…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hospira Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 21, 2014

HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) - HeartWare Battery For use as a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

HeartWare 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.