The Recall Desk

State

Oklahoma product recalls

73,738 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,822
Critical
1,040
Severe
1,493
Most recent
2026-10-28

Of the 5,822 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 1,493 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36501–36525 of 79560

  • HighFDA (Devices)·Z-1332-2019·2019-05-22

    Shippert Medical Technologies Recalls Tissu-Trans FILTRON 500 Due to Pouch Integrity Concerns

    Shippert Medical Technologies is recalling Tissu-Trans FILTRON 500 sterile pouches because a cut or hole in the packaging may compromise the product's sterility.

    Product
    Tissu-Trans FILTRON 500, Catalog 3-TT-FILTRON 500, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1320-2019·2019-05-22

    Philips SureSigns VS3 Monitor Software Defect Recall

    Philips is recalling 3,177 SureSigns VS3 monitors because a software defect prevents the device from measuring, displaying, or alarming for pulse rates above 240 beats per minute.

    Product
    SureSigns VS3 NBP, SpO2, Rec, Product Number 863072. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V389000·2019-05-22

    Volkswagen Recalls Passat and Atlas Vehicles for Headlight Adjustment Defect

    Volkswagen is recalling 2012-2020 Passat and 2018-2019 Atlas vehicles because a missing blocking cap allows headlight aim to be adjusted out of specification, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN PASSAT, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1324-2019·2019-05-22

    Philips SureSigns VS4 Monitor Software Defect Recall

    Philips is recalling 366 SureSigns VS4 monitors because software prevents the device from measuring or alarming for pulse rates above 240 beats per minute.

    Product
    SureSigns VS4 Government Bundle, Product Number 863286. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1334-2019·2019-05-22

    Shippert Medical Technologies Recalls Tissu-Trans FILTRON 2000 Medical Devices

    Shippert Medical Technologies is voluntarily recalling 6,553 units of Tissu-Trans FILTRON 2000 sterile, disposable, one-patient use devices due to a Class II classification.

    Product
    Tissu-Trans FILTRON 2000, Catalog 3-TT-FILTRON 2000, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1335-2019·2019-05-22

    Shippert Medical Technologies Recalls Tissu-Trans MEGA 1500 Due to Pouch Integrity Concerns

    Shippert Medical Technologies is recalling Tissu-Trans MEGA 1500 sterile pouches because a cut or hole may compromise sterility.

    Product
    Tissu-Trans MEGA 1500, Catalog 3-TT-MEGA 1500, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1318-2019·2019-05-22

    Philips SureSigns VS3 Monitor Software Defect Recalled

    Philips is recalling 518 SureSigns VS3 monitors because a software defect prevents the device from measuring or alarming for pulse rates above 240 beats per minute.

    Product
    SureSigns VS3 NBP Temp, Product Number 863070. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1353-2019·2019-05-22

    Abbott ARCHITECT Estradiol Reagent Kit Recall for Mifepristone Interference

    Abbott is recalling ARCHITECT Estradiol Reagent Kits because patient results may be falsely elevated for individuals currently or recently treated with Mifepristone.

    Product
    Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT Estradiol assay is a Chemiluminescent Microparticle Immunoassay (CMIA) for the quantitative determination of Estradiol in human serum and plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1350-2019·2019-05-22

    Stryker Power-LOAD Cot Fastening System Recalled for Broken Floor Plates

    Stryker is recalling 3,285 Power-LOAD Cot Fastening Systems because the floor plates holding ambulance cot anchors may be broken.

    Product
    Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1323-2019·2019-05-22

    Philips SureSigns VS4 Monitor Software Defect Recall

    Philips is recalling SureSigns VS4 monitors because software prevents the device from measuring or alarming for pulse rates above 240 beats per minute.

    Product
    SureSigns VS4 NBP, SpO2, Product Number 863283. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1331-2019·2019-05-22

    Shippert Medical Technologies Recalls Tissu-Trans FILTRON 250 Due to Pouch Integrity Concerns

    Shippert Medical Technologies is recalling Tissu-Trans FILTRON 250 sterile filters because the pouch integrity cannot be assured without visual examination.

    Product
    Tissu-Trans FILTRON 250, Catalog 3-TT-FILTRON 250, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1384-2019·2019-05-22

    AmeriHerb Blessed Thistle Herb Recalled for Potential E. coli Contamination

    AmeriHerb International Inc is recalling 108 lbs of Blessed Thistle herb due to potential contamination with generic E. coli. The product was distributed nationwide and to Canada.

    Product
    Blessed thistle herb c/s, Centaurea benedicus, Not for use during pregnancy, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1387-2019·2019-05-22

    AmeriHerb Lemon Balm Leaf Recalled for Potential E. coli Contamination

    AmeriHerb International Inc is recalling 103 lbs of Lemon Balm Leaf due to potential E. coli contamination. The product was distributed nationwide and to Canada.

    Product
    Lemon balm leaf c/s, Melissa officinalis, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1317-2019·2019-05-22

    Philips SureSigns VS3 NBP Recall for Pulse Rate Measurement Limitation

    Philips is recalling SureSigns VS3 NBP monitors because software prevents the display and alarm for pulse rates above 240 beats per minute.

    Product
    SureSigns VS3 NBP, Product Number 863069. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1342-2019·2019-05-22

    Siemens Artis Q Angiography Systems Recalled for Tabletop Movement Blockage

    Siemens is recalling 459 Artis Q angiography systems because the floating tabletop may become blocked after a collision sensor activates.

    Product
    Artis Q (material 10848280, 10848281, 10848282) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1296-2019·2019-05-22

    CVS Children's Acetaminophen Recalled for Potential B. cepacia Contamination

    Unipharma is recalling CVS Health Children's Pain & Fever Acetaminophen single-use vials due to a precautionary measure regarding potential contamination with B. cepacia bacteria.

    Product
    CVS Health Children's Pain & Fever Acetaminophen 160 mg/5 mL Pain reliever/Fever reducer Single-Use Vials Cherry Flavor 20 Single-Use Vials per carton 0.17 fl. oz. (5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, NDC 69842-0258-01, UPC 050428601891
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1329-2019·2019-05-22

    Fungitell Kit Recalled for Missing or Incorrect Components

    Associates of Cape Cod, Inc. is recalling Fungitell Kits due to potential missing or incorrect components.

    Product
    Fungitell Kit, Catalog FT001 - Product Usage: The Fungitell assay is a potease zymogen-based colorimetric assay for the qualitative detection of (1-3)Beta-D Glucan in the serum of patients with symptoms of,or medical conditions predisposing the patient to, invasive fungal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1299-2019·2019-05-22

    DrKids Children's Pain & Fever Oral Solution Recalled for B. cepacia Risk

    Unipharma, LLC is recalling 280 cartons of DrKids Children's Pain & Fever Oral Solution due to potential contamination with B. cepacia bacteria.

    Product
    DrKids Children's Pain & Fever Oral Solution Acetaminophen 160 mg/5 mL, 20 Pre-measured Single-Use Vials 0.17 fl. oz. (5 mL), Cherry Flavor, Manufactured in USA by: Unipharma, LLC. Tamarac, FL 33321, NDC 70302-011-20, UPC 370302223019
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1350-2019·2019-05-22

    Back Roads Granola Recalled for Potential Aluminum Contamination

    Back Roads Food Company is recalling specific lots of Ancient Grains Granola because the products may contain pieces of aluminum.

    Product
    Back Roads Granola: Ancient Grains Best by date: 01/11/20-02/2/20 In 10 oz, 12 oz, 2.45lb, 3 lb, and 28lb
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1297-2019·2019-05-22

    CVS Health Children's Mucus Relief Recalled for B. cepacia Contamination Risk

    Unipharma, LLC is recalling CVS Health Children's Mucus Relief Chest Congestion Plus Cough due to potential contamination with B. cepacia bacteria.

    Product
    CVS Health Children's Mucus Relief Chest Congestion Plus Cough Dextromethorphan HBr Cough Suppressant Guaifenesin Expectorant Mixed Berry Flavor 20 Singe-Use Vials Per Carton 0.17 fl. oz. (5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1306-2019·2019-05-22

    CVS Children's Cough Syrup Recalled for Potential B. cepacia Contamination

    Unipharma is recalling CVS Health Children's Cough & Chest Congestion DM due to potential contamination with B. cepacia bacteria.

    Product
    CVS Health Children's Cough & Chest Congestion DM Dextromethorphan HBr, 5 mg Cough Suppressant Guaifenesin, USP 100 mg Expectorant Mixed Berry Flavor 20 Single-Use Vials 0.17 fl. oz. (5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895,NDC 69842-262-01…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1359-2019·2019-05-22

    Barlean's Cod Liver Oil Recalled for Undeclared Sulfites

    Barlean's is recalling Cod Liver Oil softgels due to undeclared sulfites. Sulfite levels do not exceed 10 ppm.

    Product
    Item FG 10037, Barlean s Cod Liver Oil Omega 3 EPA/DHA with Added Vitamin D, 100 softgel per bottle. UPC 7 05875 61010 0
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1352-2019·2019-05-22

    Back Roads Gluten-Free Granola Recalled for Aluminum Contamination

    Back Roads Food Company is recalling specific lots of Gluten-Free Granola because the products may contain pieces of aluminum.

    Product
    Back Roads Granola: Gluten Free Best by date: 01/11/20-02/2/20 In 10 oz, 12 oz, 2.45lb, 3 lb, and 28lb
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1345-2019·2019-05-22

    MediPress Pneumatic Compression System Recalled for Missing Premarket Clearance

    Compass Health Brands is recalling MediPress pneumatic compression systems because a product design change lacked proper FDA premarket clearance.

    Product
    MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient, Model #6104M-S
    Category
    Medical Device
    Distribution
    36 states