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.

49851–49875 of 79640

  • HighFDA (Devices)·Z-0197-2017·2016-10-26

    Windstone Medical Packaging Recalls General Surgery Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling 985 general surgery kits because the Medtronic gloves included may have splits or holes that compromise sterility.

    Product
    General Plastics Pack, Kit number 008617-1 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0159-2017·2016-10-26

    Windstone C-Section Kits Recalled Due to Potential Glove Splits or Holes

    Windstone Medical Packaging is recalling C-Section kits because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    C-Section Pack, Kit number 002643-10, 002643-9, and AMS4449 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0198-2017·2016-10-26

    Windstone Medical Recalls General Surgery Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 168 General Surgery Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    General Surgery Pack, Kit number PSS1380(A convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0133-2017·2016-10-26

    Kabobs Sweet Potato Puffs Recalled Due to E. coli O121 Contamination

    Kabobs Inc is recalling Sweet Potato Puffs because they were made with flour contaminated with E. coli O121.

    Product
    SWEET POTATO PUFF, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.
    Category
    Food
    Distribution
    27 states
  • HighFDA (Devices)·Z-0224-2017·2016-10-26

    Windstone Medical Recalls Lipo Pack Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling 40 Lipo Pack kits because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Lipo Pack, Kit number AMS4420 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0267-2017·2016-10-26

    Windstone Medical Packaging Recalls Surgical Set Up Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 16 surgical Set Up Packs because they may contain defective gloves that compromise sterility.

    Product
    Set Up Pack, Kit number PSS3574(A convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0255-2017·2016-10-26

    Windstone Medical Recalls Ortho Pack Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling 92 Ortho Pack kits because they may contain defective gloves with splits or holes that compromise sterility.

    Product
    Ortho Pack, Kit number PSS3466 and PSS3466(A convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0284-2017·2016-10-26

    Windstone Medical Packaging Recalls Virginia Custom Pack Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling Virginia Custom Pack kits because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Virginia Custom Pack, Kit number RMS1744 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0167-2017·2016-10-26

    Windstone Medical Custom Surgery Kits Recalled for Sterility Compromise

    Windstone Medical Packaging recalled 56 custom surgery kits because the included Medtronic gloves may contain splits or holes, compromising sterility.

    Product
    Custom Tray, Kit numbers: PSS1836 and PSS1836(A convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0228-2017·2016-10-26

    National Foods Packaging Recalls Low Sodium Chicken Base Due to Lead

    National Foods Packaging Inc is recalling 2,000 pounds of Low Sodium Chicken Base because a spice ingredient contained elevated levels of lead.

    Product
    National Foods Packaging Low Sodium Chicken Base in 50 lb white poly-lined paper bags
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0227-2017·2016-10-26

    National Foods Packaging Recalls Chicken Base Due to Lead Contamination

    National Foods Packaging Inc is recalling 8,825 lb of Chicken Base because a spice ingredient contained elevated levels of lead. The product was distributed in Indiana, Texas, and Virginia.

    Product
    National Foods Packaging Chicken Base in 25 lb white poly-lined paper bags
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0133-2017·2016-10-26

    ConMed CORE Suction Irrigation Handpiece Recalled for Packaging Seal Crease

    ConMed is recalling CORE Suction Irrigation Handpieces because a crease in the packaging seal may create an open channel that compromises the product's sterility.

    Product
    CORE¿ Suction Irrigation Handpiece without Probe for Single Solution or Dual Bags, Catalog Number CD8302 The CORE Trumpet (CD81XX, CD83XX, and CD84XX) has applications in gynecological laparoscopy, laparoscopic cholecystectomy and other laparoscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0164-2017·2016-10-26

    Entenmann's Little Bites Chocolate Chip Muffins Recalled for Plastic Presence

    BIMBO Bakeries USA Inc. is recalling Entenmann's Little Bites Chocolate Chip Muffins due to the presence of plastic in the product.

    Product
    Entenmann's Little Bites Chocolate Chip Muffins; 10 Pouches; Net Wt. 1 lb. 0.5 OZ. ; Bimbo Bakeries USA, Inc.; PO #976, Horsham, PA 19044. Best By: October 8, 2016/3098; UPC: 7203002111; Entenmann's Little Bites Chocolate Chip Muffins; 20 Muffins, 5 Pouches; Net Wt. 8.25 OZ.…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0090-2017·2016-10-26

    Ortho-Clinical VITROS Chemistry LAC Slides Recalled Due to NAC Interference

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry LAC Slides because N-Acetylcysteine (NAC) can interfere with the assay results.

    Product
    VITROS Chemistry Products LAC Slides, REF/Product Codes 843 3880 (300 slides per sales unit) and 815 0112 (90 slides per sales unit), Unique Device Identifier Nos. 10758750004911 and 10758750004454, Rx ONLY, IVD --- For in vitro diagnostic use only. VITROS Chemistry Products…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0167-2017·2016-10-26

    Nature's One Organic PediaSmart Beverage Recalled for Incorrect Scoop Size

    Nature's One is recalling Organic PediaSmart Dairy Vanilla beverage cans because they contain a scoop that provides only 60% of the intended nutrition.

    Product
    Nature's One, Organic PediaSmart¿ Dairy Vanilla complete nutrition beverage for kids 1 to 13 years NET WT 12.7 oz (360 G) can Contains: milk, soy & coconut UPC 7 16514 88101 0 Manufactured for: Natures One, 8754 Cotter Street, Lewis Center, OH 43035
    Category
    Food
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-0129-2017·2016-10-26

    ConMed Recalls CORE Suction Irrigation Handpieces Due to Packaging Seal Creases

    ConMed is recalling CORE Suction Irrigation Handpieces because creases in the packaging seal may create open channels that compromise the product's sterility.

    Product
    CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe for Single Solution Bags, Catalog Number CD8185 The CORE Trumpet (CD81XX, CD83XX, and CD84XX) has applications in gynecological laparoscopy, laparoscopic cholecystectomy and other laparoscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0123-2017·2016-10-26

    Randox Lipase Test System Recalled for Carryover Interference

    Randox Laboratories is recalling 18 units of Lipase test kits due to carryover interference when run near LDL or Triglycerides assays.

    Product
    Randox Lipase (Colorimetric) Product Usage: A lipase test system is a device intended to measure the activity of the enzyme lipase in serum and plasma. Lipase measurements are used in the diagnosis and treatment of diseases of the pancreas such as acute pancreatitis and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0168-2017·2016-10-26

    Ozturk Gardens Recalls Black Bean and Corn Salsa Due to Elevated pH

    Ozturk Gardens is recalling 10 cases of Dr. O'z SALSA Black Bean and Corn due to elevated pH levels. The product was distributed in Oklahoma.

    Product
    "Dr. O'z SALSA Black Bean and Corn Made with my Mom's secret recipe! Stir Before Serving Net Wt. 16oz (454g) All Natural No Preservatives www.ozturkfoods.com Distributed by Ozturk Foods 28872 S. Big Hollow Rd. Park Hill OK 74451 Refrigerate After Opening"
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0134-2017·2016-10-26

    ConMed CORE Trumpet Handpiece Recalled for Packaging Seal Crease

    ConMed is recalling CORE Trumpet Handpieces because a crease in the packaging seal may create an open channel that compromises the product's sterility.

    Product
    CORE¿ Trumpet Handpiece with 5mm x 32cm Length Probe , Catalog Number CD8400 The CORE Trumpet (CD81XX, CD83XX, and CD84XX) has applications in gynecological laparoscopy, laparoscopic cholecystectomy and other laparoscopic procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0111-2017·2016-10-26

    Zimmer Biomet Recalls Vanguard Distal Femoral Augments Due to Labeling Error

    Zimmer Biomet is recalling five Vanguard Distal Femoral Augments because the product inside the carton does not match the label. The mismatched size is easily identified during surgery.

    Product
    Vanguard Distal Femoral Augment 75 X 5 RL/LM Product Usage:  Painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved.  Correction of varus, valgus, or posttraumatic deformity. …
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0132-2017·2016-10-26

    ConMed CORE Suction Irrigation Handpiece Recalled for Packaging Seal Defect

    ConMed is recalling CORE Suction Irrigation Handpieces because a crease in the packaging seal may compromise the product's sterility.

    Product
    CORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags, Catalog Number CD8300 The CORE Trumpet (CD81XX, CD83XX, and CD84XX) has applications in gynecological laparoscopy, laparoscopic cholecystectomy and other laparoscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0136-2017·2016-10-26

    Hand Biomechanics Lab Recalls Agee WristJack Fracture Reduction Systems

    Hand Biomechanics Lab Inc is recalling 65 Agee WristJack Fracture Reduction Systems because a molded beam is slightly larger than optimal, which may make surgical adjustments difficult.

    Product
    Agee-WristJack¿ Fracture Reduction System; Item number: CFD-147. The WristJack Fracture Reduction System is a fracture reduction and external fixation system for treatment of distal radius fractures. This is a single use system used for a trauma related surgery The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0166-2017·2016-10-26

    Entenmann's Little Bites Fudge Brownies Recalled Due to Plastic Presence

    BIMBO Bakeries USA is recalling Entenmann's Little Bites Fudge Brownies because plastic was found in the muffins and brownies.

    Product
    Entenmann's Little Bites Fudge Brownies - 20 muffins, 5 Pouches; Net Wt. 9.75 OZ.; Bimbo Bakeries USA, Inc., Horsham, PA 19044; Best By: October 8, 2016/3098; UPC: 7203001342
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0112-2017·2016-10-26

    Stryker Recalls Sagittal Blades Due to Potential Sterile Barrier Breach

    Stryker Instruments is voluntarily recalling 225 Sagittal Blades due to a potential sterile barrier breach in the packaging.

    Product
    Sagittal Blade 18.0X0.97X90MM, Model Number: 6118-097-090 Product Usage: Heavy duty Sagittal Blades are used to cut bone and bone related tissue in a variety of orthopedic procedures. Typical procedures include, total-knee, uni-compartmental knee, hip, shoulder and ankle…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0092-2017·2016-10-26

    Ortho VITROS URIC Slides Recalled Due to NAC Interference

    Ortho-Clinical Diagnostics is recalling VITROS URIC Slides because N-Acetylcysteine (NAC) can interfere with the assay results.

    Product
    VITROS Chemistry Products URIC Slides, REF/Product Code 194 3927 (300 slides per sales unit), Unique Device Identifier No. 10758750000340, Rx ONLY, IVD --- For in vitro diagnostic use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide