The Recall Desk

State

Oklahoma product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41701–41725 of 79629

  • LowFDA (Drugs)·D-0803-2018·2018-05-23

    Boiron Recalls Calendula Cream Due to Outer Carton Labeling Error

    Boiron Inc. is recalling 52,810 tubes of Calendula Cream because the outer carton incorrectly lists the active ingredient concentration as 7% instead of 10%.

    Product
    Calendula Cream, calendula officinalis 1X HUS-10%, 2.5 oz. tubes, Distributed by Boiron Inc., Newtown Square, PA
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0818-2018·2018-05-23

    Sun Pharma Recalls Riomet Metformin Solution Due to Labeling Errors

    Sun Pharmaceutical Industries is recalling Riomet (metformin hydrochloride) oral solution due to identified labeling discrepancies in the patient literature.

    Product
    RIOMET — RIOMET (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·18E036000·2018-05-22

    Fuel Helmets Recalls Open Face Helmets for Impact Protection Failure

    Fuel Helmets is recalling specific Open Face helmets that may not adequately protect the wearer's head in an impact, increasing the risk of injury.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18162·2018-05-22

    Porsche Recalls Wooden Toy Cars Due to Choking Hazard

    Porsche is recalling My First Porsche wooden toy cars because wheels and axles can detach, posing a choking hazard to young children.

    Product
    My First Porsche - Wooden Cars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V334000·2018-05-21

    2019 Coachmen Recreational Trailers Recalled for Incorrect Tire Placard

    Forest River is recalling 2019 Coachmen Clipper and Viking trailers because the Federal Placard lists incorrect tire pressure, which could lead to underinflation and tire failure.

    Product
    COACHMEN — COACHMEN CLIPPER, VIKING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V365000·2018-05-18

    Van-Con Recalls One 2016 School Bus Due to Roof Panel Bonding Defect

    Van-Con is recalling one 2016 33803 Dual Rear Wheel school bus because roof panel seams were not correctly bonded, posing an increased injury risk in a crash.

    Product
    VAN-CON — VAN-CON 33803 DUAL REAR-WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V332000·2018-05-17

    Chrysler Recalls Vehicles for Cruise Control Disengagement Defect

    Chrysler is recalling over 4.8 million vehicles because a wiring short may prevent the cruise control system from disengaging, increasing crash risk.

    Product
    CHRYSLER — CHRYSLER, DODGE, JEEP 300, CHALLENGER, CHEROKEE, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E033000·2018-05-17

    LuK Hybrid Propulsion System Recall for Fire Risk

    LuK is recalling hybrid propulsion systems where oil accumulation may cause an electrical short and increase fire risk. Dealers will inspect and replace components free of charge.

    Product
    HYBRID PROPULSION SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V330000·2018-05-17

    Thomas Built Buses Recalls Minotour Transit Buses for Wheelchair Lift Defect

    Daimler Trucks North America is recalling 2003-2006 Thomas Built Buses Minotour transit buses because a missing relay may allow the wheelchair lift to operate while the vehicle is moving, increasing injury risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V326000·2018-05-17

    Rebel West Powersports Recalls One 2018 Rebel R4 LSV for Missing Reflectors

    Rebel West Powersports is recalling one 2018 Rebel R4 LSV because it lacks required rear side reflex reflectors, which reduces visibility to other drivers.

    Product
    REBEL WEST POWERSPORTS — REBEL WEST POWERSPORTS REBEL R4 LSV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1393-2018·2018-05-16

    Labrada Nutrition Recalls Lean Pro 8 Cookies & Cream for Undeclared Egg

    Labrada Nutrition is recalling 132 units of Lean Pro 8 Cookies & Cream protein powder due to undeclared egg. The product was distributed in the US and internationally.

    Product
    Lean Pro 8 Cookies & Cream 1,000g (2.2lb) Tub
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V322000·2018-05-16

    McNeilus Recalls 2008-2018 Bridgemaster V Mixers Due to Tank Rupture Risk

    McNeilus is recalling 2008-2018 Bridgemaster V concrete mixers because a hydraulic tank may overpressurize and rupture, posing risks of injury and road hazards.

    Product
    MCNEILUS — MCNEILUS BRIDGEMASTER V MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1578-2018·2018-05-16

    Vyaire Medical Recalls AirLife Resuscitation Devices Due to Mask Sticking

    Vyaire Medical is recalling 20 AirLife Resuscitation Broselow Hinkle Kits because the mask component may stick, making it difficult to disconnect from the device.

    Product
    AirLife Resuscitation, Broselow Hinkle Kit Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe on their own.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1580-2018·2018-05-16

    Vyaire Medical Recalls AirLife Infant Resuscitators Due to Mask Sticking

    Vyaire Medical is recalling 198 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.

    Product
    AirLife Resuscitation, Infant, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, manometer, PEEP valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who…
    Category
    Medical Device
    Distribution
    Distributed nationwide