The Recall Desk

State

Oklahoma product recalls

73,817 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,823
Critical
1,040
Severe
1,494
Most recent
2026-11-04

Of the 5,823 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,494 (26%) are Severe.

These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50426–50450 of 79640

  • SevereFDA (Food)·F-2146-2016·2016-09-28

    Whole Foods Recalls Grassfields Leyden Cheese for E. coli Contamination Risk

    Whole Foods Market is recalling Grassfields Leyden Cheese due to possible contamination with Shiga toxin-producing E. coli (STEC). The product was sold nationwide.

    Product
    Grassfields Leyden Cheese, cut and wrapped in clear plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2352-2016·2016-09-28

    Market Basket Raw Walnuts Recalled for Listeria Contamination

    United Natural Trading is recalling Market Basket Raw Walnuts due to potential Listeria monocytogenes contamination found during third-party sampling.

    Product
    Market Basket Walnuts Raw Net Wt. 7 oz Distributed by Demoulas Supermarkets, Inc. Tewksbury, MA 01876 UPC 049705408094
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2309-2016·2016-09-28

    Eillien's Candies Recalls Sunflower Kernels Due to Listeria Risk

    Eillien's Candies is recalling various roasted sunflower kernel products because they may be contaminated with Listeria monocytogenes. No illnesses have been reported to date.

    Product
    BLAIN'S FARM & FLEET ROASTED/UNSALTED SUNFLOWER KERNEL 16 OZ, 1 LB (454 g), UPC 034952820881, Item # 699009. 10/11/16, 11/22/16, 12/30/16, 1/25/17, 2/22/16, 6/15/16, 9/16/16, 3/3/16, 5/17/16, 7/7/16, 4/20/16, 8/4/16. BULK - ROASTED/UNSALTED SUNFLOWER KERNELS 50#, 404129…
    Category
    Food
    Distribution
    10 states
  • SevereNHTSA·16E075000·2016-09-28

    Meritor Recalls 71000 and 79000 Series Axles for Insufficient Grease

    Meritor is recalling specific 71000 and 79000 Series axles manufactured in 2016 due to insufficient grease, which may cause bearing failure and increase crash risk.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2380-2016·2016-09-28

    HVL Metabolic Cleanse Recalled for Undeclared Milk Allergen

    HVL, LLC is recalling Metabolic Cleanse Revised because the product labeling fails to declare the milk allergen.

    Product
    METABOLIC CLEANSE REVISED 1181 grams, packaged in 2500cc White HDPE Canister
    Category
    Food
    Distribution
    44 states
  • HighFDA (Food)·F-2381-2016·2016-09-28

    HVL LLC Recalls Metabolic Cleanse Veg Due to Undeclared Milk Allergen

    HVL, LLC is recalling 1,635 units of Metabolic Cleanse Veg because the product labeling fails to declare a milk allergen. The product was distributed to numerous US states, Puerto Rico, Canada, and several international locations.

    Product
    METABOLIC CLEASNSE VEG 1151 grams, packaged in 2500cc White HDPE Canister
    Category
    Food
    Distribution
    44 states
  • HighFDA (Devices)·Z-2874-2016·2016-09-28

    Hospira LifeCare PCA 3 Pumps Recalled for Screw Rotation Error

    Hospira is recalling 69 LifeCare PCA 3 pumps due to a screw rotation error that stops infusion and triggers an alarm.

    Product
    LifeCare PCA 3, PCA Serial List Number 12384 Allows for clinician administration or self-administration of analgesic medications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2379-2016·2016-09-28

    HVL Ultra Protein Vanilla Recalled for Undeclared Milk Allergen

    HVL, LLC is recalling Ultra Protein Vanilla because the product labeling does not declare the milk allergen.

    Product
    ULTRA PROTEIN VANILLA¿ 948 grams, packaged in 2500cc White HDPE Canister
    Category
    Food
    Distribution
    44 states
  • HighFDA (Food)·F-2332-2016·2016-09-28

    Immune Tree Recalls Colostrum Capsules Due to Undeclared Milk Allergen

    Immune Tree is recalling specific colostrum capsule products because they contain an undeclared milk allergen. Consumers should stop using the affected items.

    Product
    Colostrum6 Capsules 500mg, Item No 9901, 180 ct. Sold under the brands: Immune Tree, Immune Pro-6 (Not purchased since 8/25/2014), Surthrival, Good For You Canada. Packaged using HDPE White bottle, except Surthrival which uses a Brown HDPE Bottle
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2334-2016·2016-09-28

    Immune Tree Recalls Colostrum Products Due to Undeclared Milk Allergen

    Immune Tree is recalling specific colostrum products because they contain undeclared milk, a major food allergen.

    Product
    LeptiTrim6 Vanilla Shake Item No. 9907; 860 g. Brand Immune Tree; Packaged using HDPE White bottle
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2848-2016·2016-09-28

    Smith & Nephew Recalls Renasys Sterile Transparent Film Due to Seal Failures

    Smith & Nephew is recalling Renasys Sterile Transparent Film and related dressing kits because sterility seal integrity failures may compromise the sterile barrier.

    Product
    RENASYS Sterile Transparent Film and all the RENASYS Dressing kits that contains the RENASYS Sterile Transparent Film Is intended for patients who would benefit from a suction device (negative pressure) to help promote wound healing by removing fluids including irrigation and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2849-2016·2016-09-28

    TriMed Recalls Semi-Tubular Plates Due to Screw Failure During Implantation

    Trimed Inc is recalling 30 units of SMTP-10 Semi-Tubular Plates because a non-locking screw passed through a plate hole during implantation.

    Product
    TriMed Semi-Tubular Plate, 10-Hole, Model No. SMTP-10 Contoured plate with offset screw holes. The plate is 103 mm in length, 1.3 mm thick and 9.6 mm wide. The part is made of surgical steel conformance with ASTM F138 or F139. The plate is used to fixation of long bone…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2871-2016·2016-09-28

    Merge Healthcare Recalls CADstream MRI Software Due to Grid Selection Error

    Merge Healthcare is recalling CADstream software versions 4.1.3 and prior because an incorrect grid selection could lead to an incorrect biopsy or missed target during MRI analysis.

    Product
    CADstream software. Product Usage: CADstream is an image processing system designed to assist in the visualization, analysis, and reporting of magnetic resonance imaging (MRI) studies. CADstream also is intended to provide workflow efficiency and interventional planning…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V699000·2016-09-28

    Newmar Recalls Canyon Star RVs Due to Wheelchair Door Defect

    Newmar is recalling 2015-2017 Canyon Star recreational vehicles because the wheelchair access door may open while driving, increasing crash risk.

    Product
    NEWMAR — NEWMAR CANYON STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2333-2016·2016-09-28

    Immune Tree Recalls Colostrum Powder Due to Undeclared Milk Allergen

    Immune Tree is recalling specific colostrum powder products because they contain undeclared milk, a major food allergen.

    Product
    Colostrum6 Powder (6.5 oz) Item No. 9902; Sold under the following brands: Immune Tree, Surthrival, HealthWorks (Not purchased since 3/18/15). Packaged in HDPE White bottle, except Surthrival which uses a Brown HDPE Bottle
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2335-2016·2016-09-28

    Immune Tree Recalls Colostrum Powder Due to Undeclared Milk Allergen

    Immune Tree is recalling specific colostrum powder products because they contain undeclared milk, a major food allergen.

    Product
    Colostrum6 Powder Kilo (35.3 oz); Item No. 9903; Brand Name Immune Tree, Surthrival, Packaged using HDPE White bottle, except Surthrival which uses a Brown HDPE Bottle
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2866-2016·2016-09-28

    Sorin S5 Heart-Lung Machine Recalled for Power Supply Failure Risk

    Sorin Group USA is recalling 5,264 Stöckert S5 Heart-Lung Machines worldwide due to a potential failure of the Uninterruptible Power Supply.

    Product
    St¿ckert S5 System, S5 Heart-lung machine, Cardiopulmonary bypass heart-lung machine console Product Usage: The St¿ckert S5 System is intended to be used during cardiopulmonary bypass for procedures lasting six (6) hours or less. These devices come in direct contact with the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V698000·2016-09-28

    Ford Recalls 2013-2017 Focus Hatchbacks for Latch Defect

    Ford is recalling 2013-2017 Focus hatchbacks with manual transmissions because the rear hatch may unlatch with a single button press, increasing injury risk.

    Product
    FORD — FORD FOCUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2842-2016·2016-09-28

    Philips HeartStart MRx Monitor/Defibrillator Recall for Handle Separation

    Philips is recalling 394 HeartStart MRx Monitor/Defibrillators because the handle can separate from the housing due to broken mounts.

    Product
    HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2084-2016·2016-09-28

    Campbell's SpaghettiOs Recalled for Potential Choking Hazard from Plastic Pieces

    Campbell Soup Supply Co. is recalling 14,789 cases of SpaghettiOs due to a potential choking hazard from red plastic pieces found in the cans.

    Product
    Campbell's SpaghettiOs Original Pasta in Tomato and Cheese Sauce Net Wt. 14.2 ounces in metal cans, NDC: 0-51000-22432-3
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-2330-2016·2016-09-28

    Southern Grove Cashews Recalled for Possible Peanut Presence

    Kanan Enterprises is recalling Southern Grove Cashews with Sea Salt due to the possible presence of peanuts. The product was distributed in Ohio, Kansas, and Minnesota.

    Product
    Southern Grove Cashews with Sea Salt, a 10 ounce stand up pouch bag with a UPC 0 38445 12286 5 and the date codes of Best By May 24 2017 KN and August 05 2017 KN
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2336-2016·2016-09-28

    Immune Tree Recalls Colostrum Powder Due to Undeclared Milk Allergen

    Immune Tree is recalling specific colostrum powder products because they contain undeclared milk, a major food allergen.

    Product
    Colostrum6 Powder (2.5 oz), Item No. 9915, Sold under brand Immune Tree (discontinued), Packaged using HDPE White bottle
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2855-2016·2016-09-28

    Abbott Recalls SENSAR Intraocular Lenses Due to Mislabeled Units

    Abbott Medical Optics is recalling 84 SENSAR Foldable Intraocular Lenses because they were not checked prior to release, which may result in the release of mislabeled units.

    Product
    SENSAR Foldable IOL with OptiEdge Design, Model No. AR40e The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2867-2016·2016-09-28

    Invivo Recalls Philips Expression IP5 MRI Patient Monitoring Units

    Invivo Corporation is recalling 639 Philips Expression Information Portal (IP5) units because display numerics may freeze and menu keys may disable after extended run time.

    Product
    Philips Expression Information Portal (IP5) Model 865471. The IP5 is intended to be used as a secondary display control unit for the Expression MRI Patient Monitoring System and the Expression MR200 MRI Patient Monitoring System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2872-2016·2016-09-28

    McKesson Radiology Software Recalled for Missing STAT Priority Icon

    McKesson Medical Imaging Group is recalling McKesson Radiology software versions 12.1.1 and 12.2 because the STAT priority icon was not displayed in the Study List when a study was opened.

    Product
    McKesson Radiology, versions 12.1.1 and 12.2 McKesson Radiology (MR) is a Picture Archiving Communication System (PACS). It is a medical image and information management application that is intended to receive, transmit, store, retrieve, display, print and process digital…
    Category
    Medical Device
    Distribution
    40 states