The Recall Desk

State

Oklahoma product recalls

73,737 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.

These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33901–33925 of 79559

  • LowFDA (Drugs)·D-0303-2020·2019-11-13

    Sato Pharmaceutical Recalls Sankaijo Botanical Laxative Tablets

    Sato Pharmaceutical Inc. is recalling Sankaijo Botanical Laxative tablets because the sennosides content is lower than the labeled claim.

    Product
    SANKAIJO — SANKAIJO (DOCUSATE SODIUM, SENNOSIDES)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V806000·2019-11-12

    Aston Martin Recalls DB11, Vantage, and DBS Superleggera for Air Bag Defect

    Aston Martin is recalling 2018-2019 DB11, Vantage, and DBS Superleggera vehicles because passenger air bag fasteners may not be tightened properly, increasing injury risk in a crash.

    Product
    ASTON MARTIN — ASTON MARTIN DBS SUPERLEGGERA, VANTAGE, DB11
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V805000·2019-11-12

    Ford Recalls 2019-2020 F-150 Trucks for Battery Cable Fastener Issue

    Ford is recalling 2019-2020 F-150 vehicles because a battery cable fastener may loosen, potentially causing engine stalling, loss of braking or steering assist, or fire.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V809000·2019-11-12

    Ford Recalls 2016-2017 Lincoln MKX Vehicles for Battery Cable Fire Risk

    Ford is recalling 2016-2017 Lincoln MKX vehicles with 3.7L engines because the battery cable harness may contact a bracket, causing a short circuit and increasing fire risk.

    Product
    LINCOLN — LINCOLN MKX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E076000·2019-11-12

    Matrix Alpha Motorcycle Helmets Recalled for Retention System Failure

    Matrix Headgear is recalling Alpha motorcycle helmets because the retention system may fail, allowing the helmet to separate from the head during a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V807000·2019-11-08

    Nissan Recalls Murano, Maxima, Pathfinder, QX60 for Brake Fire Risk

    Nissan is recalling 391,479 vehicles because brake fluid may leak onto an electrical circuit board, creating a fire risk.

    Product
    NISSAN — NISSAN, INFINITI MURANO, QX60, MAXIMA, PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V804000·2019-11-08

    Mitsubishi i-MiEV Recall for Brake Vacuum Pump Corrosion Risk

    Mitsubishi is recalling 2012-2017 i-MiEV vehicles because water may corrode the brake vacuum pump, causing a loss of braking assist and increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI I-MIEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-110819·2019-11-08

    USDA Issues Public Health Alert for Ready-to-Eat Entrees Due to Listeria Risk

    USDA FSIS issued a public health alert for specific ready-to-eat entrees containing ingredients recalled by Mann's Packing Co. due to possible Listeria monocytogenes contamination.

    Product
    FSIS Issues Public Health Alert for Ready-to-Eat Entrees due to Possible Listeria Monocytogenes Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V803000·2019-11-07

    Freightliner Cascadia Recall for Brake Chamber Clearance Defect

    Daimler Trucks North America is recalling 2020 Freightliner Cascadia vehicles because brake chambers may contact the frame rail, potentially causing detachment and reduced braking.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V798000·2019-11-07

    NHTSA Recalls 2019 Mercedes-Benz and Freightliner Sprinter Diesel Fuel Systems

    NHTSA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because a fuel system defect may cause diesel leaks or fuel overflow.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V802000·2019-11-07

    Hyundai Recalls 2020 Palisade Vehicles for Side Air Bag Defect

    Hyundai is recalling 2020 Palisade vehicles because mounting bolts may damage side curtain air bags, potentially preventing proper inflation in a crash.

    Product
    HYUNDAI — HYUNDAI PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V801000·2019-11-07

    GM Recalls 2014-2016 Chevrolet SS for Steering Connector Corrosion

    General Motors is recalling 2014-2016 Chevrolet SS vehicles because corrosion in the steering connector may cause a loss of electric power steering assist, increasing the risk of a crash.

    Product
    CHEVROLET — CHEVROLET CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V799000·2019-11-07

    Thor Motor Coach Recalls Tuscany and Venetian Motorhomes for Visibility Defect

    Thor Motor Coach is recalling specific Tuscany and Venetian motorhomes because rear reflectors may be positioned too high, reducing vehicle visibility and increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY, TUSCANY XTE, VENETIAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0203-2020·2019-11-06

    Ethicon Echelon Flex Powered Plus Stapler Recalled for Anvil Defect

    Ethicon Endo-Surgery Inc is recalling 2,112 Echelon Flex Powered Plus ENDOPATH 60mm Staplers worldwide due to out-of-specification anvil components that may compromise staple line integrity.

    Product
    ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 340mm shaft, Product Code PSEE60A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0160-2020·2019-11-06

    Innoveix Recalls Lyophilized Human Chorionic Gonadotropin Due to Sterility Concerns

    Innoveix Pharmaceuticals is recalling 290 vials of Lyophilized Human Chorionic Gonadotropin 5,500 USP Units due to a lack of sterility assurance.

    Product
    Lyophilized Human Chorionic Gonadotropin 5,500 USP Units For injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0201-2020·2019-11-06

    Ethicon Recalls ECHELON FLEX Staplers Due to Anvil Defect

    Ethicon Endo-Surgery Inc is recalling 255 units of the ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler because an out-of-specification anvil may cause malformed staples and compromised staple lines.

    Product
    ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 280mm shaft, Product Code PCEE60A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0221-2020·2019-11-06

    Thoratec CentriMag Motor Recalled Due to Electromagnetic Interference Issues

    Thoratec is recalling CentriMag Acute Circulatory Support System motors due to reports of motor and pump issues caused by electromagnetic interference.

    Product
    CentriMag Acute Circulatory Support System Motor, U.S. Model 102956 and OUS Model 201-10002, a component of the CentriMag Extracorporeal Blood Pumping System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0200-2020·2019-11-06

    Ethicon Echelon Flex Endopath Stapler Recall for Out-of-Spec Anvil

    Ethicon is recalling Echelon Flex Endopath 60mm Staplers due to out-of-specification anvil components that may compromise staple line integrity.

    Product
    ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft, Product Code EC60A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·108-2019·2019-11-06

    Simmons Prepared Foods Recalls Poultry Products Due to Metal Contamination

    Simmons Prepared Foods is recalling approximately 2.07 million pounds of poultry products that may contain metal. The products were shipped to institutions in eight states.

    Product
    Simmons Prepared Foods, Inc. — Simmons Prepared Foods, Inc. Recalls Poultry Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0159-2020·2019-11-06

    Innoveix Recalls Lyophilized Sermorelin Injection Due to Sterility Concerns

    Innoveix Pharmaceuticals is recalling 1,747 vials of compounded Sermorelin injection because the product lacks sterility assurance.

    Product
    Lyophilized Sermorelin w/ GHRP2 3 mg For injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0158-2020·2019-11-06

    Innoveix Recalls Lyophilized Human Chorionic Gonadotropin Due to Sterility Concerns

    Innoveix Pharmaceuticals is recalling 413 vials of Lyophilized Human Chorionic Gonadotropin 5,000 USP Units due to a lack of sterility assurance.

    Product
    Lyophilized Human Chorionic Gonadotropin 5,000 USP Units For injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0157-2020·2019-11-06

    Innoveix Recalls Lyophilized Chorionic Gonadotropin Due to Sterility Concerns

    Innoveix Pharmaceuticals is recalling 3,905 vials of Lyophilized Chorionic Gonadotropin 11,000 USP Units for Injection due to a lack of sterility assurance.

    Product
    Lyophilized Chorionic Gonadotropin 11,000 USP Units for Injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910
    Category
    Drug
    Distribution
    Distributed nationwide