All recall categories

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.

Medical devices

Reported Jan 20, 2016

Medrad Source Administration Sets, Catalog number INT CSS. For use with MEDRAD Intego PET Infusion pump Systems, in…

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

Bayer Healthcare

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo), 9mm, 11mm, 13mm, 15mm, and 17mm

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

Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical…

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

Skytron, Div. The KMW Group, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

Reprocessed Stryker Color Cuff and Color Cuff II Adult Tourniquet Cuffs Model Numbers: 5921-218-135, 5921-044-135,…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

Zimmer, Virage OCT Spinal Fixation System, Item Number: 07.01738.001, a posterior system intended to achieve an implant…

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

Zimmer Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 13, 2016

Software version VD10E for Syngo X-Workplace; Picture archiving and communication system.

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 6, 2016

Cross Valley Farms cucumbers, 24 count corrugated carton

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

Del Monte Fresh Produce N A Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 6, 2016

MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Vancomycin Screen Agar

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

Becton Dickinson & Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for…

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

Biomerieux

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization and fixation of fractures, revision…

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

Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Boston Scientific, Chariot ST-CCV Guiding Sheath, Sterilized using ethylene oxide: Product Description Material Number…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Optional PS500 Power Supply Unit for the Evita V500 Ventilator and Babylog VN500 Ventilator. Babylog VN500 is a…

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

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Reagent Management System (RMS) Dimension EXL with LM Product Usage: The Reagent Management System (RMS) is a module…

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

Siemens Healthcare Diagnostics Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2015

MYLA CLINIC PATCH 3.2.0 CD Product Usage: MYLA is a computer application (Middleware) based on Web 2.0 technology…

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

bioMerieux, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2015

MOSAIQ Oncology Information System. Used to manage workflows for treatment planning and delivery.

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2015

Unolok Blunt Fill Needle 18G x 1.5" Red, Sterile, Single use, Non-injectable needle, Single use, non-injection needle

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

Myco Medical Supplies Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2015

Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column

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

Teleflex Medical

FDA (openFDA device enforcement)

Food

Reported Dec 9, 2015

Founders Pride Chocolate Chip Cookies 120 - 2.5 oz frozen dough pieces packaged per case, Net Wt. 18.75 lbs. (8.50 Kg.)…

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

Custom Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 9, 2015

Radiesse (+) Lidocaine Injectable Implant 1.5cc, P/N: 8063M0K1. Indicated for subdermal implantation for the correction…

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

Merz North America, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 9, 2015

Goodcents deli fresh subs Fresh Baked Giant Cookie, Chocolate Chip Cookie, Serving Size: 1 Cookie, Approx. NET WT. 2.5…

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

Mr Goodcents Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 9, 2015

Melissa's Italian Pine Nuts, 2oz (57g), 12 cartons/case, UPC 0 45255 14351 5 Melissa's Profit Strip Pine Nuts Italy,…

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

World Variety Produce Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 2, 2015

Daily Chef Peanut Butter Bars, Net Wt. 27 oz (1 lb 11 oz) 765g, Made in Canada, Manufactured for: CSM Bakery Products…

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

CSM Bakery Products NA

FDA (openFDA food enforcement)

Food

Reported Dec 2, 2015

M&M Old Fashioned Gourmet Cookie Dough NET WT. 3 lb. (48 oz.) Distributed By: Tower Cafe, Okarche, OK 73762 packaged in…

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

Tower Cafe Inc. dba Okarche Bakery

3 more products in this recall

FDA (openFDA food enforcement)

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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.