The Recall Desk

State

Oklahoma product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45776–45800 of 79632

  • ModerateFDA (Devices)·Z-2745-2017·2017-07-26

    Pentax Medical Recalls Laryngeal Strobe Systems Due to Missing Transformers

    Pentax Medical is recalling 241 laryngeal strobe systems because they were not always provided with required 9175 isolation transformers.

    Product
    9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is used to electronically record, display, transfer, and store digital video data of laryngeal or pharyngeal structures, and audio data, for medical and pedagogical applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2743-2017·2017-07-26

    Pentax 9310HD Digital Video Capture Modules Recalled for Missing Transformers

    Pentax of America is recalling 241 units of 9310HD Digital Video Capture Modules because they were not always provided with required 9175 isolation transformers.

    Product
    9310HD Digital Video Capture Modules Product Usage: The 9310HD is used to electronically record, display, transfer, and store digital video data of laryngeal or pharyngeal structures, and audio data, for medical and pedagogical applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0980-2017·2017-07-26

    Hospira Recalls Argatroban Injection Due to Impurity Specification Failure

    Hospira is recalling 701 vials of Argatroban Injection because a denitroquinoline-related impurity exceeded specifications during testing.

    Product
    Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 5 mL Single-use vial, Rx Only, Sterile, Manufactured by: Gland Pharma Limited, Hyderabad, India, Manufactured for: Hospira, Inc, Lake Forest, IL 60045 --- NDC 0409-1140-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0981-2017·2017-07-26

    Shionogi Recalls Mefenamic Acid Capsules for Dissolution Failures

    Shionogi Inc. is recalling Mefenamic Acid 250mg capsules because stability testing showed low dissolution results.

    Product
    Mefenamic Acid, 250mg capsules, packaged in 30-count bottles, Rx Only, Distributed by: Prasco Laboratories Mason, OH 45040 USA, Manufactured by: Halo Pharmaceutical Inc. Whippany, NJ 07981, NDC 66993-070-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0983-2017·2017-07-26

    Teva Recalls Buprenorphine and Naloxone Tablets Due to Impurities

    Teva Pharmaceuticals is recalling specific lots of Buprenorphine and Naloxone Sublingual Tablets because they failed impurity specifications.

    Product
    Buprenorphine and Naloxone Sublingual Tablets, 2 mg/0.5 mg 30 tablets per bottle, Rx only, Distributed by: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-5720-56
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0998-2017·2017-07-26

    Obagi-C Rx Night Cream Recalled for Missing Safety Information

    Valeant Pharmaceuticals is recalling 844 bottles of Obagi-C Rx System C-Therapy Night Cream because the bottles are missing the product insert and outer carton containing safety instructions.

    Product
    Obagi-C Rx System C-Therapy Night Cream, Net wt. 2 oz. (57g) bottle, Rx only, Distributed by OMP, Inc., Long Beach, CA Made in USA, NDC 62032-222-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0982-2017·2017-07-26

    Shionogi Recalls PONSTEL Capsules Due to Failed Dissolution Specifications

    Shionogi Inc. is recalling 455 bottles of PONSTEL capsules because stability testing showed low dissolution results.

    Product
    PONSTEL (Mefanamic Acid) USP, 250 mg capsules, 30-count bottles, Rx Only, Manufactured for: Shionogi Inc. Florham Park, NJ 07932 Manufactured by: Halo Pharmaceutical Inc. Whippany, NJ 07981
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·17195·2017-07-25

    Polaris Recalls RZR 170 Vehicles Due to Fuel Leak and Fire Hazards

    Polaris is recalling 16,800 RZR 170 recreational off-highway vehicles because fuel tank necks can crack or wiring can overheat, posing fire risks.

    Product
    RZR 170 recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V472000·2017-07-25

    Ford Recalls 2014-2015 Vehicles Due to Improper Seat Bolts

    Ford is recalling 94,605 vehicles because improperly manufactured bolts may fracture, increasing injury risk in a crash.

    Product
    FORD — FORD, LINCOLN ESCAPE, F-150, E-350, MKC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·085-2017·2017-07-25

    D & D Foods Recalls Pepperoni Pizza Due to Undeclared Soy Allergen

    D & D Foods is recalling approximately 17,847 pounds of Hy-Vee pepperoni pizza products because they contain undeclared soy lecithin, a known allergen.

    Product
    D & D Foods, Inc. Recalls Pizza Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17193·2017-07-24

    iRover Recalls Self-Balancing Scooters Due to Fire and Explosion Hazard

    iRover is recalling about 2,800 self-balancing scooters because their lithium-ion batteries can overheat, smoke, catch fire, or explode. No injuries or property damage have been reported.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V468000·2017-07-22

    Piaggio Recalls 2014-2017 Fly 150 3V Scooters for Brake Defect

    Piaggio is recalling 2014-2017 Fly 150 3V scooters because front brake disc mounting screws may loosen, potentially causing the front wheel to lock up and increasing crash risk.

    Product
    PIAGGIO — PIAGGIO FLY 150 3V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V467000·2017-07-21

    BMW Recalls 2017 C Evolution and C650 GT Scooters for Rim Marking Defect

    BMW is recalling 2017 C Evolution and C650 GT scooters because front rims may lack required markings, which could lead to incorrect tire installation and handling issues.

    Product
    BMW — BMW C EVOLUTION, C650 GT MAXI-SCOOTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V464000·2017-07-20

    Tremcar Recalls Rear Impact Guards on Certain Trailers

    Tremcar is recalling rear impact guards on specific trailers because they may not adequately resist force in a crash, increasing the risk of injury.

    Product
    TREMCAR — TREMCAR 1625FT3 VAC TANDEM, 2800FT3 DRY BULK QUAD, 1350FT3 B-TRAIN PUP, 2300FT3 QUAD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V460000·2017-07-20

    Spartan Motors Recalls 2015-2017 Aeromaster Vehicles for Wiper Motor Defect

    Spartan Motors is recalling 2015-2017 Utilimaster Aeromaster vehicles because a missing ground wire may cause intermittent loss of windshield wiper function, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER AEROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide