The Recall Desk

State

Oklahoma product recalls

73,509 recalls have nationwide distribution and so reach Oklahoma. 5,818 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,818
Critical
1,043
Severe
1,490
Most recent
2026-10-14

Of the 5,818 recalls naming Oklahoma we have scored against our rubric, 1,043 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,490 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,818 recalls whose distribution notice names Oklahoma specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24451–24475 of 79327

  • HighFDA (Devices)·Z-0200-2022·2021-11-10

    Artis zeego X-Ray System Software Error Affects Image Reconstruction

    Siemens Artis zeego fluoroscopic X-ray systems have a software error that incorrectly displays 3D image reconstruction when the patient table is rotated more than 4 degrees, potentially resulting in incorrect patient treatment during image-guided procedures.

    Product
    Artis zeego, Fluoroscopic X-Ray System Models: 10280959,10502505, 10848283 in combination with the following workplace/system application software models: Product/Model #: syngo X Workplace, 10281061 syngo X Workplace, 10281299 syngo X Workplace, 10502522 Syngo Application…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0082-2022·2021-11-10

    Hamburger buns recalled due to Listeria and Salmonella contamination risk

    Kansas City LLC., operating as Best Harvest Bakeries, is recalling hamburger buns distributed to restaurants across 15 states due to positive environmental samples for Listeria and Salmonella species.

    Product
    Hamburger buns, 5" in unlabeled clear plastic bags, 30 or 12 buns per bag.
    Category
    Food
    Distribution
    15 states
  • HighNHTSA·21V870000·2021-11-10

    Ford recalls 2021 Explorer and Lincoln Aviator suspension modules

    Ford is recalling certain 2021 Explorer and Lincoln Aviator vehicles with incorrect rear suspension module components due to a labeling error. The defect may affect vehicle handling, ride height, and braking, increasing crash risk.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0079-2022·2021-11-10

    Hotdog Buns Recall Due to Potential Listeria and Salmonella Contamination

    Kansas City LLC., DBA Best Harvest Bakeries is recalling hotdog buns distributed to restaurants across 15 US states due to positive environmental samples for Listeria and Salmonella species.

    Product
    Hotdog buns, customer specified formula, in unlabeled clear plastic bags, 30 or 12 buns per bag.
    Category
    Food
    Distribution
    15 states
  • HighCPSC·22017·2021-11-10

    Hart 18-Gauge 2" Brad Nailers Recalled for Involuntary Nail Discharge

    Hart Consumer Products is recalling about 15,700 Hart 18-Gauge 2" Brad Nailers because the contact sensor can malfunction and cause the tool to involuntarily discharge a nail, posing a risk of serious injury.

    Product
    Hart 18-Gauge 2" Brad Nailers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0190-2022·2021-11-10

    Arietta 850 Ultrasound Software Displays Cardiology Measurements Incorrectly

    FujiFilm Arietta 850 ultrasound systems with affected software versions display cardiology measurement results incorrectly. The recall affects 38 units distributed nationwide.

    Product
    Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0081-2022·2021-11-10

    Hamburger buns recalled for potential Listeria and Salmonella contamination

    Kansas City LLC., doing business as Best Harvest Bakeries, is recalling hamburger buns distributed to restaurants across multiple states due to positive environmental samples for Listeria and Salmonella species.

    Product
    Hamburger buns, 4.5" in unlabeled clear plastic bags, 30 or 12 buns per bag.
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-0189-2022·2021-11-10

    Arietta 750 Ultrasound Software Versions Affected by Incorrect Measurement Display

    FujiFilm Healthcare is recalling Arietta 750 Ultrasound Software versions V1.0.0 through V2.1.3 due to measurement display errors in critical cardiology functions that could lead to incorrect clinical diagnoses. The instruction manual also contains an error.

    Product
    Arietta 750 Ultrasound Software Version: V1.0.0 through V2.1.3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0192-2022·2021-11-10

    Arietta 65 Ultrasound Software: Calculation Error in EROA Diagnostic Measurements

    Arietta 65 Ultrasound systems with software versions 1.0 through 4.0.0 contain a calculation error that produces incorrect measurements of cardiac valve function during diagnostic assessments.

    Product
    Arietta 65 Ultrasound Software Versions: V1.0 through V4.0.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0196-2022·2021-11-10

    ADVIA Centaur SARS-CoV-2 Antigen Assay Recalled for Insufficient Validation Data

    Siemens Healthcare Diagnostics is recalling 261 ADVIA Centaur SARS-CoV-2 Antigen Assay test kits distributed nationwide because the FDA determined that validation data submitted for emergency authorization was insufficient to confirm the assay's effectiveness.

    Product
    ADVIA Centaur SARS-CoV-2 Antigen Assay (100 Test Kit), SMN # 11207866
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0188-2022·2021-11-10

    FDA Recalls 3M Red Dot ECG Monitoring Electrodes Due to Potential Carbon Stud Breakage

    3M Red Dot ECG monitoring electrodes (Catalog No. 2244) are being recalled due to potential breakage of the carbon stud from the eyelet. Approximately 2,081,000 units distributed nationwide and internationally are affected.

    Product
    3M Red Dot Electrodes, Radiolucent Monitoring Electrode with Foam Tape, Catalog No. 2244, (3M ID (SKU): 70-2011-8506-6, SAP ID: 7100212989), packaged 10 electrodes per card, 5 cards per pouch, 20 pouches per shipper box, 1,000 electrodes total per shipper box. The 3M Red Dot…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0095-2022·2021-11-10

    Pharmanex Kids Jungamals dietary supplement missing fish allergen label

    NSE Products, Inc. is recalling Pharmanex Kids Jungamals dietary supplement because the label does not disclose fish allergen present in the product's Vitamin E ingredient.

    Product
    Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tablets, white bottle, NSE Products Inc., Provo, UT 84601 1-888-PHARMANEX
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0080-2022·2021-11-10

    Hamburger Buns Recalled for Listeria and Salmonella Contamination Risk

    Kansas City LLC., DBA Best Harvest Bakeries is recalling approximately 10,712 hamburger buns distributed to restaurants across 14 states due to positive environmental samples for Listeria and Salmonella.

    Product
    Hamburger buns, 4" in unlabeled clear plastic bags, 30 or 12 buns per bag.
    Category
    Food
    Distribution
    15 states
  • HighFDA (Drugs)·D-0086-2022·2021-11-10

    Lupin Irbesartan Tablets Recalled for Impurity Contamination

    Lupin Pharmaceuticals is recalling Irbesartan 75 mg tablets due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient. The recall affects 51,144 bottles distributed nationwide.

    Product
    IRBESARTAN — IRBESARTAN (IRBESARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0203-2022·2021-11-10

    Dental Implants Mislabeled as Smaller Size; Risk of Nerve Damage

    GM Helix Acqua Implant dental implants were mislabeled as a smaller size. If incorrectly installed in cases with low bone quality, they could damage the nerve or adjacent bone structures.

    Product
    GM Helix Acqua Implant 3.5x10, Article No. 140.944
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0198-2022·2021-11-10

    Dental implant recalled due to size mismatch with labeling

    Implant Direct Sybron Manufacturing is recalling 83 dental implants from lot 166300 because the implants differ in size from what is labeled on the packaging. The implants were distributed across multiple US states and Japan.

    Product
    ImplantDirect, REF 834713, Legacy 2 Implant 4.7mmD x 13mmL, 4.5mmD Platform,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22013·2021-11-10

    ABUS MountZ Youth Helmets Recalled for Head Injury Risk

    ABUS is recalling about 790 MountZ youth helmets that do not meet U.S. safety standards for bicycle helmets. The helmets pose a risk of head injury and should be returned for a full refund.

    Product
    ABUS MountZ Youth Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0197-2022·2021-11-10

    Dental implants recalled for size mismatch with package labeling

    Implant Direct is recalling 61 dental implants because the packaged implants are a different size than declared on the labeling. Patients who may have received these implants should contact their healthcare provider.

    Product
    ImplantDirect, REF 834711, Legacy 2 Implant 4.7mmD x 11.5mmL, 4.5mmD Platform,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0199-2022·2021-11-10

    MEDRAD Twist & Go Syringe Recalled Due to Labeling Error

    Bayer Medical Care is recalling 6,950 units of MEDRAD Twist & Go Disposable Syringes due to labeling errors that could cause confusion about syringe compatibility with the MEDRAD Mark 7 Arterion Injection System.

    Product
    The MEDRAD Twist & Go Disposable Syringe 150 mL with Quick Fill Tube is a syringe made from a clear polycarbonate material and is an accessory to the MEDRAD Mark 7 Arterion Injection System. It is designed to be loaded into the injector head of the injection system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0083-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Failed Excipient Specifications

    Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin Tablets (10 mg/80 mg) because the product was manufactured using an excipient that failed to meet conductivity specifications.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0090-2022·2021-11-10

    Starbucks Doubleshot Espresso canned coffee recall due to sealing defect

    PepsiCo is recalling Starbucks Doubleshot Espresso canned coffee products due to inadequate sealing that may lead to premature spoilage. The recall affects approximately 85,956 cases distributed nationwide.

    Product
    Starbucks Doubleshot Espresso, Espresso & Light Cream, 6.5 FL OZ UPC 012000008801
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0082-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Failed Excipient Specifications

    Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin Tablets (10 mg/20 mg) nationwide because the product was manufactured using an excipient that failed conductivity specifications.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0084-2022·2021-11-10

    Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled for Failed Excipient Specifications

    Dr. Reddy's Laboratories is recalling Ezetimibe and Simvastatin 10 mg/40 mg tablets because an excipient used in manufacturing failed conductivity specifications. The recall affects 11,590 bottles of 30-count and 3,585 bottles of 90-count packages distributed nationwide.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0202-2022·2021-11-10

    Aspiration Syringe Kit MVSK60 Inadvertently Shipped with OUS Labeling

    MicroVention's Aspiration Syringe Kit (REF: MVSK60) was labeled for international distribution but inadvertently shipped to U.S. customers. The affected lot (H2146461) was distributed to Alabama, Nevada, and New York.

    Product
    Aspiration Syringe Kit, REF: MVSK60
    Category
    Medical Device
    Distribution
    Distributed nationwide