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.

Which agencies issued them

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.

48651–48675 of 79640

  • HighFDA (Devices)·Z-0941-2017·2017-01-11

    Interventional Spine Recalls G3 Opticage Expandable Interbody Fusion Devices

    Interventional Spine Inc is recalling 239 G3 Opticage Expandable Interbody Fusion Devices because the proximal end may separate during implantation, preventing the device from expanding.

    Product
    G3 Opticage Expandable Interbody Fusion Device, Model No. 9180-00, 9180-01, 9180-06, 9180-07, 9180-17, 9101-00, 9101-06 The Opticage Expandable Interbody Fusion Device is a posterior lumbar intervertebral body fusion device and is indicated for use with autogenous bone graft in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0342-2017·2017-01-11

    Wells Pharmacy Recalls B-Complex Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling B-complex + Vit C injectable vials due to a lack of assurance of sterility.

    Product
    B-complex + Vit C 20 mg/mL Injectable, 30 mL vial, Compounded by Wells Pharmacy Network, LLC, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0382-2017·2017-01-11

    Wells Pharmacy Recalls Nandrolone Decanoate Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling 526 vials of compounded Nandrolone Decanoate injectable nationwide due to a lack of assurance of sterility.

    Product
    Nandrolone Decanote (H), 200 mg/mL Injectable, 10 mL vial, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0947-2017·2017-01-11

    Aesculap Recalls Gomco Circumcision Clamps Due to Excessive Bleeding Reports

    Aesculap Implant Systems LLC is recalling 437 units of Gomco Circumcision Clamps nationwide after receiving complaints of excessive bleeding following use.

    Product
    Gomco Circumcision Clamps with separate O-Ring Component: The device is packaged non-sterile and has no shelf-life The Gomco clamp is intended to be used for circumcision surgeries
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0948-2017·2017-01-11

    Tepha GalaSHAPE 3D Medical Device Recalled for Endotoxin Specification Exceedance

    Tepha Incorporated is recalling 29 units of GalaSHAPE 3D medical devices because endotoxin levels slightly exceeded specifications.

    Product
    GalaSHAPE 3D; product code SH3D03, a medium size oval GalaSHAPE" 3D is indicated for use as a bioresorbable scaffold for soft tissue support and to repair, elevate and reinforce deficiencies where weakness or voids exist that require the addition of material to obtain the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0949-2017·2017-01-11

    Merit PreludeEASE Hydrophilic Sheath Introducer Dilator Recall

    Merit Medical Systems is recalling 335 PreludeEASE Hydrophilic Sheath Introducer Dilators because the tips are undersized and cannot pass a 0.021-inch guide wire.

    Product
    PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE Hydrophilic Sheath Introducer is intended to provide access and facilitate the percutaneous introduction of various devices into veins and/or arteries, including but not limited to the radial artery, while…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0326-2017·2017-01-11

    Qualitest Recalls Temazepam Capsules Due to Failed Stability Specifications

    Vintage Pharmaceuticals is recalling 1,200 bottles of Temazepam 7.5 mg capsules because they failed stability specifications. The affected lot is distributed nationwide.

    Product
    TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-5891-21
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17V020000·2017-01-10

    BMW Recalls X5 and X6 Models for Air Bag Inflator Rupture Risk

    BMW is recalling 2007-2012 X5 and X6 vehicles because the front passenger air bag inflators may rupture during a crash, potentially causing serious injury or death.

    Product
    BMW — BMW X6, X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17V029000·2017-01-10

    Honda and Acura Recall Vehicles for Front Passenger Air Bag Inflator Defect

    Honda is recalling specific Acura and Honda models because front passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    ACURA — ACURA, HONDA RL, ELEMENT, RIDGELINE, MDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V016000·2017-01-10

    Subaru and Saab Recall Vehicles Due to Air Bag Inflator Rupture Risk

    Subaru is recalling 2005-2008 models and 2006 Saab 9-2X vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    SUBARU — SUBARU, SAAB BAJA, IMPREZA, 9-2X, TRIBECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V017000·2017-01-10

    Mercedes-Benz Recalls Vehicles for Front Passenger Air Bag Inflator Rupture Risk

    Mercedes-Benz is recalling specific 2008-2012 models because front passenger air bag inflators may rupture during deployment, potentially sending metal fragments into the vehicle.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ E550, C63, C250, C300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V015000·2017-01-10

    Land Rover Recalls Range Rovers for Air Bag Inflator Rupture Risk

    Jaguar Land Rover is recalling 2007-2012 Range Rovers because front passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V030000·2017-01-10

    Honda Recalls Vehicles for Front Passenger Air Bag Inflator Rupture Risk

    Honda is recalling specific 2006-2012 models because the front passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    HONDA — HONDA, ACURA CIVIC, CIVIC HYBRID, TSX SPORT WAGON, INSIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·003-2017·2017-01-10

    Perfect Fit Meals Recalls Chicken Breast Due to Undeclared Allergens

    Perfect Fit Meals is recalling approximately 3,546 pounds of chicken breast product because it contains undeclared milk and wheat allergens.

    Product
    Perfect Fit Meals, LLC Recalls Chicken Breast Product Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V013000·2017-01-10

    Mazda Recalls B-Series Trucks Due to Air Bag Inflator Rupture Risk

    Mazda is recalling 2007-2009 B-Series trucks because the passenger air bag inflator may rupture in a crash, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA B-SERIES TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V024000·2017-01-10

    Ford Recalls Vehicles for Air Bag Inflator Rupture Risk

    Ford is recalling specific 2005-2012 vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    LINCOLN — LINCOLN, FORD, MERCURY ZEPHYR, MKZ, GT, MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V028000·2017-01-10

    Nissan Recalls Infiniti and Versa Models for Air Bag Inflator Rupture Risk

    Nissan is recalling specific Infiniti and Nissan Versa vehicles because the front passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    INFINITI — INFINITI, NISSAN FX35, FX45, M35, VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17065·2017-01-10

    Michaels Recalls Rock Salt Lamps Due to Shock and Fire Hazards

    Michaels is recalling about 80,000 Lumière brand rock salt lamps because the dimmer switch or outlet plug can overheat, posing shock and fire risks.

    Product
    Rock Salt Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide