The Recall Desk

State

Oklahoma product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52401–52425 of 79647

  • HighCPSC·16194·2016-06-10

    Auldey Toys Recalls Sky Rover Toys Due to Fire Hazard

    Auldey Toys is recalling Sky Rover toys because the included yellow USB charging cords can overheat, posing fire and burn hazards.

    Product
    Sky Rover toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V422000·2016-06-10

    GM Recalls 2013-2016 Chevrolet Vehicles for Missing Seatbelt Warning Chime

    General Motors is recalling specific Chevrolet Spark, Sonic, and Trax vehicles because the radio software may fail to provide audible seatbelt or key-in-ignition warnings.

    Product
    CHEVROLET — CHEVROLET SPARK, SONIC, TRAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V417000·2016-06-09

    Honda Recalls 2015-2016 Odyssey, MDX, and Pilot for Fuel Tank Welds

    Honda is recalling specific 2015-2016 Odyssey, Acura MDX, and Pilot vehicles because fuel tank welds may separate, causing a leak that could lead to a fire.

    Product
    HONDA — HONDA, ACURA ODYSSEY, MDX, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V418000·2016-06-09

    Daimler Recalls 2008-2009 Sterling Bullet Trucks Due to Air Bag Defect

    Daimler Trucks is recalling 2008-2009 Sterling Bullet 4500 and 5500 chassis cabs because passenger air bag inflators may rupture, posing a risk of serious injury or death.

    Product
    STERLING — STERLING BULLET 5500, BULLET 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E054000·2016-06-09

    Ontario Recalls EVOS Full Face Modular Helmets for Safety Standard Failures

    1888653 Ontario Inc. is recalling specific EVOS Full Face Modular Helmets that may not adequately protect the wearer's head in a crash and lack required safety labeling.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V419000·2016-06-09

    Forest River Recalls 2017 Georgetown Motorhomes Due to Overloading Risk

    Forest River is recalling 2017 Georgetown motorhomes because extra seat belts allow more passengers than the vehicle's weight rating supports, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V416000·2016-06-09

    Daimler Trucks Recalls 2017 Freightliner and Western Star Models for Engine Stall Risk

    Daimler Trucks is recalling specific 2017 Freightliner, Western Star, and FCCC trucks because an engine control module defect may cause the engine to stall without restarting, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR, FCCC CASCADIA, 122SD, 4900, XCM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16191·2016-06-09

    Rhino Metals Recalls Bighorn Handgun Safes Due to Security Flaw

    Rhino Metals is recalling Bighorn P-20 handgun security safes because they can be opened without a combination, posing a serious risk of injury to children and others.

    Product
    Bighorn handgun security safes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V420000·2016-06-09

    Toyota Recalls Vehicles with Incorrect Load Carrying Capacity Labels

    Southeast Toyota Distributors is recalling 2015-2016 Toyota and Scion vehicles because the load carrying capacity label may be incorrect, potentially leading to vehicle overload.

    Product
    TOYOTA — TOYOTA, SCION TUNDRA, TC, HIGHLANDER, FR-S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V415000·2016-06-09

    Audi Recalls 2007-2009 A8 and S8 Models for Sunroof Glass Defect

    Volkswagen Group of America is recalling 2007-2009 Audi A8 and S8 vehicles because the sunroof glass may not be properly secured and could detach while driving.

    Product
    AUDI — AUDI S8, A8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0949-2016·2016-06-08

    Akorn Recalls Sulfacetamide Sodium Ophthalmic Solution Due to Sterility Concerns

    Akorn, Inc. is recalling specific lots of Sulfacetamide Sodium Ophthalmic Solution because they failed antimicrobial effectiveness testing, raising concerns about sterility.

    Product
    Sulfacetamide Sodium Ophthalmic Solution, USP, 10%, Sterile, Rx Only, 15 mL bottles, Mfd. by: Akorn, Inc., Lake Forest, IL 60045 --- NDC 17478-221-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0910-2016·2016-06-08

    FDA Recalls Unapproved Ligandrol Supplements Sold Nationwide and in Brazil

    Invisiblu International LLC is recalling LGD-Xtreme capsules containing unapproved ligandrol because the product was marketed without an approved NDA or ANDA.

    Product
    LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1849-2016·2016-06-08

    Curity All Purpose Sponges Recalled Due to Compromised Sterility

    FDA is recalling Curity All Purpose Sponges due to compromised sterility from a barrier breach. The recall affects units distributed in the US and 20 other countries.

    Product
    Curity All Purpose Sponges, Non-woven, 4 Ply, Soft Pouch, 4" x 4" (10.2 cm x 10.2 cm) Item Number: 8047
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1859-2016·2016-06-08

    Recall of Vistec X-Ray Detectable Sponges Due to Sterility Breach

    Covidien LLC is recalling Vistec X-Ray Detectable Sponges because a breach of the barrier packaging may have compromised sterility.

    Product
    Vistec X-Ray Detectable Sponges, 26 Ply, 8" x 4" (20.3 cm x 10.2 cm) Item Number: 7321
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1855-2016·2016-06-08

    Curity X-Ray Detectable Laparotomy Sponges Recalled for Sterility Breach

    The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.

    Product
    Curity X-Ray Detectable Laparotomy Sponges, Soft Pouch Pack, 12" x 12" (30.5 cm x 30.5 cm) Item Number:6534
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1847-2016·2016-06-08

    Curity Gauze Sponges Recalled for Compromised Sterility

    Covidien LLC is recalling Curity Gauze Sponges because a breach of the barrier packaging may have compromised their sterility.

    Product
    Curity Gauze Sponges, 16 ply 4" x 4" (10.2 cm x 10.2 cm), Sterile 10's in Soft Pouch; Item Number: 397310; Open mesh fabric intended to be used to inside the body or a surgical incision to control bleeding, absorb fluid, or protect organs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V411000·2016-06-08

    Forest River Recalls 2015 Glaval Synergy Buses for Steering Defect

    Forest River is recalling 2015 Glaval Synergy transit buses because steering boxes may wear prematurely, risking loss of steering control.

    Product
    GLAVAL BUS — GLAVAL BUS SYNERGY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1852-2016·2016-06-08

    Curity X-Ray Detectable Laparotomy Sponges Recalled for Sterility Breach

    The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.

    Product
    Curity X-Ray Detectable Laparotomy Sponges, Tray Pack, 18" x 18" (45.7 cm x 45.7 cm) Item Number: 6022
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1405-2016·2016-06-08

    Angel Wings and Magzuma Supplements Recalled for Undeclared Milk and Soy

    Liquid Assets Inc. is recalling Angel Wings and Magzuma dietary supplements because they contain undeclared milk and soy allergens.

    Product
    Angel Wings Complete Daily Multi with 146 nutrients including Anti-aging and Superfruit Antioxidants and 75 Plant Derived Minerals 120 Capsules UPC: 0-16158-01225-3 Liquid Assets, Inc. Tulsa, OK 74116 1-888-497-4535 www.ExceptionalProducts.org; Magzuma Zuma Supreme Daily…
    Category
    Food
    Distribution
    43 states
  • SevereFDA (Devices)·Z-1853-2016·2016-06-08

    Curity X-Ray Detectable Laparotomy Sponges Recalled for Sterility Breach

    FDA is recalling Curity X-Ray Detectable Laparotomy Sponges due to compromised sterility from a barrier breach.

    Product
    Curity X-Ray Detectable Laparotomy Sponges, Tray Pack, 8" x 36" (20.3 cm x 91.4 cm Item Number: 6056
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V413000·2016-06-08

    Terex Advance Recalls 2016 Concrete Mixer Trucks Due to Chute Failure

    Terex Advance is recalling 338 model year 2016 Front Discharge Concrete Mixer trucks because a weld failure could cause the main chute to detach while driving, increasing crash risk.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE CONCRETE
    Category
    Vehicle
    Distribution
    Distributed nationwide