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.

48701–48725 of 79640

  • HighFDA (Devices)·Z-0909-2017·2017-01-04

    GE Healthcare Recalls Legacy Systems Due to CRT Monitor Fall Risk

    GE Healthcare is recalling Legacy and other imaging systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.

    Product
    Legacy
    Category
    Medical Device
    Distribution
    41 states
  • ModerateFDA (Food)·F-0906-2017·2017-01-04

    Bio-Botanica Recalls Vitamin D-3 Drops for Excess Dosage

    Bio-Botanica is recalling Nature's Answer and Seeking Health Vitamin D-3 drops because the lots contain more Vitamin D3 than the label claims.

    Product
    Liquid VITAMIN D-3 Drops distributed under the following private labels and sizes: a) NATURE'S ANSWER VITAMIN D-3 DROPS DIETARY SUPPLEMENT, 0.5 FLUID OZ/15 mL, UPC 8300026132 -- Nature's Answer Hauppauge, NY 11788; and b) Seeking Health Optimal Vitamin D, Liquid Vitamin D-3…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0240-2017·2017-01-04

    Virtus Pharmaceuticals Recalls Virt-Select Prenatal Softgels Due to GMP Deviations

    Virtus Pharmaceuticals is recalling Virt-Select Prenatal/Postnatal Softgels because the active ingredient manufacturer is on an FDA Import Alert for cGMP deviations.

    Product
    Virt-Select Prenatal/Postnatal Softgels, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based DHA , packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-249-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0903-2017·2017-01-04

    Ortho-Clinical Diagnostics Recalls VITROS Intact PTH Reagent Packs

    Ortho-Clinical Diagnostics is recalling VITROS Intact PTH Reagent Packs due to a positive bias of up to 20% and an incorrectly set reference interval.

    Product
    VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN 10758750006287 / Product Code 6802892 - Reagent Pack, 2) UPN 10758750006250 / Product Code 6802893 - Calibrators For the quantitative measurement of intact parathyroid hormone (iPTH) in human serum and plasma…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0241-2017·2017-01-04

    VirtPrex Prenatal Tablets Recalled Due to API Manufacturer Import Alert

    Virtus Pharmaceuticals is recalling VirtPrex Prenatal/Postnatal Tablets because the active ingredient manufacturer is on an FDA Import Alert.

    Product
    VirtPrex Prenatal/Postnatal Tablets, Prescription Supplement Containing Folic Acid and DHA, packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-348-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0235-2017·2017-01-04

    Care-Tech Recalls Surgical Hand Scrub Due to Labeling and Cap Defects

    Care-Tech Laboratories is recalling Techni-Care Surgical Hand Scrub because bottles have missing or illegible lot and expiration dates, as well as defective or cracked caps.

    Product
    Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation (3.0% w/v Chloroxylenol), packaged in a) 4 oz. bottles (NDC 46706-201-01), b) 8 oz bottles (NDC 46706-201-02), c) 16 oz. bottles (NDC 46706-201-03), d) 12 oz. pumpette (NDC 46706-201-05), e) 32 oz. bottles…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0239-2017·2017-01-04

    Virtus Pharmaceuticals Recalls Extra-Virt Plus DHA Prenatal Softgels

    Virtus Pharmaceuticals is recalling 2,406 bottles of Extra-Virt Plus DHA Prenatal/Postnatal Softgels because the API manufacturer is on FDA Import Alert.

    Product
    Extra-Virt Plus DHA Prenatal/Postnatal Softgel, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based DHA , packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-251-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0238-2017·2017-01-04

    Virt-Advance Prenatal Softgels Recalled Due to API Manufacturer Import Alert

    Virtus Pharmaceuticals is recalling Virt-Advance Prenatal/Postnatal Softgels because the active ingredient manufacturer is on an FDA Import Alert.

    Product
    Virt-Advance Prenatal/Postnatal Softgels, Prescription Folic Acid Containing Dietary Supplement, packaged in 90-count bottle, Rx only, Made in Canada, NDC 76439-357-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17E001000·2017-01-03

    Takata Frontal Passenger Air Bag Inflator Rupture Recall

    Takata is recalling certain frontal passenger air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17E002000·2017-01-03

    Takata Frontal Passenger Air Bag Inflator Module Recall

    Takata is recalling specific frontal passenger air bag inflators in 2012 vehicles registered in 14 states and territories due to a risk of rupture.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V002000·2017-01-03

    Audi Recalls 2012-2017 Models for Coolant Pump Fire Risk

    Volkswagen Group of America is recalling specific Audi models because a blocked coolant pump can overheat and cause a fire.

    Product
    AUDI — AUDI A4 ALLROAD, A6, Q5, A5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V001000·2017-01-03

    Audi Recalls 2011-2017 Q5 Vehicles Due to Side Air Bag Corrosion Risk

    Volkswagen Group of America is recalling 2011-2017 Audi Q5 vehicles because water in the sunroof drainage system may corrode side air bag inflators, posing a risk of serious injury.

    Product
    AUDI — AUDI Q5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V957000·2016-12-31

    Forest River Recalls 2017 Fifth-Wheel RVs Due to Door Hinge Defect

    Forest River is recalling 2017 XLR Toyhauler and Prime Time Spartan fifth-wheel vehicles because rear cargo door hinge welds may be insufficient, increasing the risk of personal injury.

    Product
    PRIME TIME — PRIME TIME, FOREST RIVER SPARTAN, XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V946000·2016-12-30

    Porsche Recalls 2017 Models Due to Side Air Bag Defect

    Porsche is recalling 2017 911, 718 Cayman, and 718 Boxster vehicles because the side air bag inflator initiator may fail to ignite during a crash.

    Product
    PORSCHE — PORSCHE 911, 718 CAYMAN, 718 BOXSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V956000·2016-12-30

    Hyundai Recalls 2017 Sonata and Elantra for Air Bag Defect

    Hyundai is recalling 2017 Sonata and Elantra vehicles because the driver's air bag inflator seal may be improperly installed, potentially reducing protection in a crash.

    Product
    HYUNDAI — HYUNDAI SONATA, ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16C009000·2016-12-30

    4moms Recalls Self-Installing Infant Car Seats Due to Attachment Defect

    4moms is recalling specific Self Installing Rear-facing Infant Car Seats because a tight rivet may prevent the carrier from securely attaching to the base, increasing injury risk in a crash.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V945000·2016-12-29

    Ford Recalls 2017 F-250 and F-350 Trucks for Fuel Tank Strap Defect

    Ford is recalling 2017 F-250 and F-350 Super Duty trucks because a missing frame reinforcement bracket may allow the fuel tank strap to separate, increasing fire risk.

    Product
    FORD — FORD F-350 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V944000·2016-12-29

    Glacier Recalls 2016 RV Explorers Due to Axle Bolt Defect

    Glacier is recalling 38 model year 2016 RV Explorer trailers because a short axle bolt may fail, causing the wheel assembly to detach and increasing crash risk.

    Product
    GLACIER — GLACIER RV EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V942000·2016-12-29

    Land Rover Recalls Vehicles for Defective Seatbelt Pretensioners

    Jaguar Land Rover is recalling 2016-2017 Range Rover, Range Rover Sport, and 2017 Discovery Sport vehicles because front seatbelt pretensioners may not function properly in a crash.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT, RANGE ROVER, DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V943000·2016-12-29

    Jaguar Recalls 2016-2017 XJ Models Due to Air Bag Defect

    Jaguar is recalling 2016-2017 XJ vehicles because the front passenger air bag may fail to deploy in a crash. Dealers will replace the air bag free of charge.

    Product
    JAGUAR — JAGUAR XJ
    Category
    Vehicle
    Distribution
    Distributed nationwide