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 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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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.