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.

49151–49175 of 79640

  • HighNHTSA·16V869000·2016-12-02

    Thor Motor Coach Recalls 2017 Quantum RQ29 Motorhomes for Missing Light

    Thor Motor Coach is recalling 32 model year 2017 Quantum RQ29 motorhomes because they may be missing a required mid-ship marker light, which can increase crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH QUANTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V867000·2016-12-02

    Mitsubishi Recalls Outlander Sport Vehicles for Lift Gate Corrosion Risk

    Mitsubishi is recalling 2011-2012 and 2016 Outlander Sport vehicles because the lift gate support tube may corrode, causing the gate to fall suddenly and increase injury risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17717·2016-12-01

    Lexibook Baby Bath Seats Recalled for Drowning Hazard

    CPSC recalls about 7,000 Lexibook baby bath seats and chairs because they can tip over, posing a drowning hazard to babies.

    Product
    Lexibook® Baby Bath Seats and Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17042·2016-12-01

    TCP LED Lamps Recalled for Electrical Shock Hazard

    Technical Consumer Products is recalling about 39,000 LED lamps sold at Habitat for Humanity in California due to an electrical shock hazard.

    Product
    Technical Consumer Products (TCP) LED lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V865000·2016-12-01

    Livin' Lite Recalls 2017 RVs Due to Fire Risk from Gas Line

    Livin' Lite is recalling 2017 Camplight and Quicksilver RVs because a rubber propane gas line can melt and cause a fire. Dealers will replace the line with a copper extension.

    Product
    LIVIN LITE — LIVIN LITE CAMPLIGHT, QUICKSILVER 6.0
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E088000·2016-12-01

    Lippert Brake Axle Recall for Potential Brake Lockup or Failure

    Lippert Components is recalling specific 7000lb and 8000lb Brake Axles because loose flange nuts may cause brakes to lock up or fail to engage, increasing crash risk.

    Product
    SERVICE BRAKES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0479-2017·2016-11-30

    Blue Bunny Ice Cream Recalled for Listeria Contamination Risk

    Wells Enterprises is recalling specific lots of Blue Bunny Hoppin' Holidoodle ice cream due to potential Listeria monocytogenes contamination.

    Product
    Blue Bunny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz. UPC 070640014644 and UPC 070640014651 (high altitude).
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0153-2017·2016-11-30

    Hospira Recalls Fentanyl Citrate Injection Ampules Due to Broken Tips

    Hospira is recalling specific lots of Fentanyl Citrate Injection ampules because broken tips may compromise sterility.

    Product
    Fentanyl Citrate Injection, USP, 100 mcg Fentanyl/ 2mL, Single Dose, 50 mcg/mL, Rx only, Hospira, Inc., Lake Forest IL 60045, NDC 0409-4093-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0653-2017·2016-11-30

    AtriCure Recalls COBRA Fusion Ablation Systems Due to Component Separation Risk

    AtriCure is recalling COBRA Fusion Ablation Systems because a part may separate and remain in the body, potentially causing permanent impairment or damage.

    Product
    COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model Numbers: 700-001, 700-001S, 700-001MI, 700-002, and 700-003. Intended to ablate cardiac tissue during cardiac surgery using radiofrequency (RF) energy when…
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Food)·F-0527-2017·2016-11-30

    Free2b Sun Cups Chocolate Recalled for Potential Milk Contamination

    Seth Ellis Chocolatier is recalling Free2b Sun Cups Chocolate due to potential contamination with milk ingredients. The recall covers 189 master cases distributed nationwide.

    Product
    Free2b Sun Cups Chocolate. Made With SunButter Sunflower Spread. Packaged in 2 Cups. Net weight 1.5 oz (45g) and 1 Cup. Net weight 0.75 oz (21g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0146-2017·2016-11-30

    VistaPharm Recalls Lactulose Solution Due to Bacterial Contamination

    VistaPharm is recalling Lactulose Solution, USP, 10 g/15 mL, because bulk solution tested positive for Burkholderia cepacia bacteria.

    Product
    Lactulose Solution, USP, 10 g/15 mL, 15 mL unit dose cups (NDC 66689-039-01), packaged in 15 mL x 50 unit dose cups per case (NDC 66689-039-50), Rx only, Manufactured by VistaPharm, Inc., Largo, FL 33771.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0635-2017·2016-11-30

    Merit Medical Procedure Kits Recalled for Compromised Sterile Barrier

    Merit Medical Systems is recalling 53 Procedure Kits due to a compromised sterile barrier. The kits were distributed nationwide to specific states and Japan.

    Product
    Procedure Kit. Catalog Numbers K12-04830B and K12-YP030A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0655-2017·2016-11-30

    Hologic Recalls SURESOUND22 Uterine Sounds Due to Sterile Barrier Breach

    Hologic is recalling SURESOUND22 uterine sound multipacks because a breach in the sterile barrier compromises product sterility.

    Product
    SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices. SURESOUND22 Multipack (OUS Distribution) containing 2 packs of six devices. For uterine sound
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0530-2017·2016-11-30

    EN-R-G Foods Recalls Protein Chews Due to Nausea and Vomiting Complaints

    EN-R-G Foods is recalling Cherry Lime, Raspberry, and Juneberry Protein Chews due to consumer complaints of nausea and vomiting after consumption.

    Product
    Protein Chews Raspberry,1.8oz, film package, 12 packets per box.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0632-2017·2016-11-30

    Merit Medical Recalls Manifold Kits Due to Compromised Sterile Barrier

    Merit Medical Systems is recalling 40 Manifold Kits (Catalog No. K09-11867AP) because the sterile barrier is compromised, posing a risk of infection.

    Product
    Manifold Kit. Catalog Number K09-11867AP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0634-2017·2016-11-30

    Merit Medical Recalls Pressure Monitoring Kits Due to Sterile Barrier Compromise

    Merit Medical Systems is voluntarily recalling 130 MeriTrans Pressure Monitoring Kits because a compromised sterile barrier may affect product sterility.

    Product
    Pressure Monitoring Kit (MeriTrans"). Catalog Number K11-00232G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0622-2017·2016-11-30

    Toshiba Aquilion Prime CT System Recalled for Cooling Oil Leak Risk

    Toshiba American Medical Systems is recalling Aquilion Prime CT systems because cooling oil in the x-ray tube heat exchanger may leak during operation.

    Product
    Aquilion Prime TSX-303A Aquilion PRIME is a multislice helical CT system with an 40-row detector. High-speed rotation allows rapid data acquisition and shortens scan times, while the fast reconstruction unit further improves throughput, reducing the time required for diagnosis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V861000·2016-11-30

    Cummins Recalls 2015-2016 Generator Sets Due to Door Hinge Failure Risk

    Cummins is recalling 164 model year 2015-2016 generator sets because door hinges may fail, causing doors to detach and create road hazards.

    Product
    CUMMINS POWER GENERATION — CUMMINS POWER GENERATION GENERATOR SET
    Category
    Vehicle
    Distribution
    Distributed nationwide