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 6, 2015
MicroScan -Neg Breakpoint Combo Panel Type 34; Catalog number B1017-404; Panel MicroScan Neg Breakpoint 34 Neg panels…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported May 6, 2015
CD99 Catalog number PM008 AA; For In Vitro Diagnostic Use. Product Usage: Provides adjunctive diagnostic information…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biocare Medical, LLC
FDA (openFDA device enforcement)
Reported May 6, 2015
Woodsmen's American Seasoning Net Weight 13 oz; and 3.2 oz Distributed by: WOODSMEN'S AMERICAN SEASONING, LINESVILLE,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Con Yeager Spice Co.
29 more products in this recall
FDA (openFDA food enforcement)
Reported May 6, 2015
Caviwave Pro Ultrasonic Cleaning System, Product Usage: To wash (remove tissue, blood and other contaminants) or dry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2015
Equinoxe 44mm Short Humeral Head Catalog Number 310-01-44. Orthopedic shoulder implant component.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Apr 29, 2015
The PCA 3 infusion pump allows clinicians, or patients, to (self) Administer analgesia safely and effectively within…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 23, 2015
West Liberty Foods Recalls Grilled Chicken Breast Products Due to Possible Foreign Matter Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.West Liberty Foods LLC
USDA FSIS
Reported Apr 22, 2015
LOW PROFILE NON-LOCK SCREW; 2.7mm x 22 mm; REF 131227222; LOT RM105E. Provides the orthopaedic surgeon a means of bone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Apr 22, 2015
Potassium Chloride, microencapsulated extended-release tablets, 20 mEq, blister card of 30/10 cards in a corrugated…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cardinal Health
FDA (openFDA drug enforcement)
Reported Apr 22, 2015
WALLACH LL 100 cryosurgical units: LL100 Cryosurgical - Part Number 900001; LL110 with Pinned Yoke - Part Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Apr 22, 2015
Kraft Macaroni & Cheese Boxed Dinner Original Flavor, 7.25oz.,packaged in blue and yellow cardboard box. There are four…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods Group Inc.
FDA (openFDA food enforcement)
Reported Apr 22, 2015
PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs, 60 Pure Caps HDPE bottle
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ReNew Life Formulas, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 22, 2015
Talon Grasping Device, 160 cm, US endoscopy. Used for retrieval of foreign bodies, tissue specimens, stones or calculi…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Reported Apr 15, 2015
CS 8100, CATALOG # (s): 5303045, 5311129, 5303060, 5303110 Intended to produce complete or segmented tomographic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 15, 2015
KETOROLAC TROM 30 MG/ML INJ, 1 mL glass vials repackaged individually inside an amber glass bottle, packaged by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RemedyRepack Inc.
FDA (openFDA drug enforcement)
Reported Apr 15, 2015
Texamerican Chili Powder: 5 lbs. Item Number: ARCH064-50; 10 lbs. Item Number: TF5002 (R&D only).
High riskUsing this product could cause serious injury, illness or death — stop using it now.Texamerican Food Blending, Inc.
7 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 8, 2015
BD FACSCalibur; Catalog Numbers 342973, 342975, 34976 In vitro Diagnostics Use.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BD Biosciences, Systems & Reagents
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2015
ToggleLoc; fastener, fixation, non degradable, soft tissue; Artificial Ligament Fixation Device #7 PE Ziploop Extended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Bard 100% Latex-Free Urinary Drainage Bag with Anti-Reflux Chamber and Bard EX-Lok Sampling; Product Code 154006: Lot #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
GE Healthcare, Aespire 7900, Aespire View Anesthesia Machines. Model numbers 1009-9012-000. Intended to provide general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Mrs. Fields White Chunk Macadamia Cookies; 12 individually wrapped cookies in a tray/box; there are 6 trays/boxes to a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Interbake Foods LLC
FDA (openFDA food enforcement)
Reported Apr 8, 2015
Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc. Cardiac Rhythm Disease Management
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm; The 130 Degree Aiming Arm and 125 Degree Aiming Arm are a part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, 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.