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.

42076–42100 of 79629

  • CriticalFDA (Food)·F-1383-2018·2018-04-25

    Nutrizone Recalls Nirvanio Green Malay Kratom Due to Salmonella Risk

    Nutrizone LLC is recalling all packages of Nirvanio Green Malay Kratom because dietary supplements have the potential to be contaminated with Salmonella.

    Product
    Nirvanio Green Malay Kratom all packages, all quantities
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1382-2018·2018-04-25

    Nutrizone LLC Recalls Nirvanio Bali Kratom Due to Salmonella Risk

    Nutrizone LLC is recalling all packages of Nirvanio Bali Kratom because dietary supplements may be contaminated with Salmonella.

    Product
    Nirvanio Bali Kratom all packages, all quantities
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V264000·2018-04-25

    Blue Bird Recalls 2018-2019 Transit Buses Due to Air Brake Gauge Defect

    Blue Bird is recalling 2018-2019 All American and Vision transit buses because air brake gauges may incorrectly display 0 PSI, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1409-2018·2018-04-25

    Philips Brilliance iCT SP CT Systems Recalled for Emergency Stop Defect

    Philips is recalling 19 Brilliance iCT SP CT systems because closing the emergency stop may disable the horizontal motor, allowing the couch to move during patient loading.

    Product
    Brilliance iCT SP - Model no. 728311 Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V263000·2018-04-25

    Blue Bird Recalls 2018-2019 School Buses for Air Brake Gauge Defect

    Blue Bird is recalling 2018-2019 Vision and All American school buses because air brake gauges may incorrectly display 0 PSI, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1386-2018·2018-04-25

    Nutrizone Recalls Pain Out Green Malay Kratom Due to Salmonella Risk

    Nutrizone LLC is recalling all packages of Pain Out Green Malay Kratom because dietary supplements can be contaminated with Salmonella.

    Product
    Pain Out Green Malay Kratom all packages, all quantities
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0684-2018·2018-04-25

    Lupin Recalls Cefdinir Powder for Oral Suspension Due to Superpotency

    Lupin Pharmaceuticals is voluntarily recalling 40,824 bottles of Cefdinir powder for oral suspension because the drug was found to be superpotent.

    Product
    CEFDINIR — CEFDINIR (CEFDINIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1384-2018·2018-04-25

    Nutrizone Recalls Nirvanio Maeng Da Kratom Due to Salmonella Risk

    Nutrizone LLC is recalling all packages of Nirvanio Maeng Da Kratom because dietary supplements have the potential to be contaminated with Salmonella.

    Product
    Nirvanio Maeng Da Kratom all packages, all quantities
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1388-2018·2018-04-25

    Nutrizone LLC Recalls Pain Out Thai Kratom Due to Salmonella Risk

    Nutrizone LLC is recalling all packages of Pain Out Thai Kratom because dietary supplements may be contaminated with Salmonella.

    Product
    Pain Out Thai Kratom all packages, all quantities
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1379-2018·2018-04-25

    Nutrizone Recalls Cali Green Malay Kratom Due to Salmonella Risk

    Nutrizone LLC is recalling all packages of Cali Green Malay Kratom because dietary supplements may be contaminated with Salmonella.

    Product
    Cali Green Malay Kratom all packages, all quantities
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1387-2018·2018-04-25

    Nutrizone Recalls Pain Out Maeng Da Kratom Supplements Nationwide

    Nutrizone LLC is recalling all packages of Pain Out Maeng Da Kratom dietary supplements nationwide due to the potential for Salmonella contamination.

    Product
    Pain Out Maeng Da Kratom all packages, all quantities
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1381-2018·2018-04-25

    Nutrizone LLC Recalls Cali Thai Kratom Due to Salmonella Risk

    Nutrizone LLC is recalling all packages of Cali Thai Kratom because dietary supplements may be contaminated with Salmonella.

    Product
    Cali Thai Kratom all packages, all quantities
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1385-2018·2018-04-25

    Nutrizone Recalls Nirvanio Kratom Supplements Due to Salmonella Risk

    Nutrizone LLC is recalling all packages of Nirvanio Special Reserve Kratom because dietary supplements can be contaminated with Salmonella.

    Product
    Nirvanio Special Reserve Kratom all packages, all quantities
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1380-2018·2018-04-25

    Nutrizone Recalls Cali Maeng Da Kratom Supplements Nationwide

    Nutrizone LLC is recalling all packages of Cali Maeng Da Kratom dietary supplements nationwide due to the potential for Salmonella contamination.

    Product
    Cali Maeng Da Kratom all packages, all quantities
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V261000·2018-04-25

    Lakota Recalls 2018-2019 Trailers Due to Ramp Bolt Failure Risk

    Lakota is recalling 2018-2019 Bighorn, Charger, and Colt trailers because ramp-securing bolts may loosen or break, increasing the risk of injury or a crash.

    Product
    LAKOTA — LAKOTA COLT, BIGHORN, CHARGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1020-2018·2018-04-25

    Divinity Kratom Capsules Recalled Due to Unapproved New Dietary Ingredient

    Divinity Product Distribution LLC is recalling kratom capsules because the ingredient lacks adequate safety information to ensure it does not present a significant risk of illness or injury.

    Product
    Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC, Blue Springs, MO 64015; 2) Divinity Bali Kratom, 10PK Capsules; 3) Divinity Bali Kratom, 20PK Capsules; 4) Divinity Bali Kratom, 40PK Capsules;
    Category
    Food
    Distribution
    44 states
  • SevereFDA (Food)·F-1021-2018·2018-04-25

    Kratom Powder Recalled Due to Inadequate Safety Information for New Ingredient

    Divinity Product Distribution LLC is recalling kratom powder products because the ingredient lacks sufficient safety data to ensure it does not pose a risk of illness or injury.

    Product
    Kratom powder labeled in the following ways 1) Enhance Your Life, Kratom Essence Maeng Da Mitragyna speciosa, 150 gras; 2) Bali Kratom, 15 g Powdered; 3) Bali Kratom, 30 g Powdered; 4) Bali Kratom, 60 g Powdered; 5) Bali Kratom, 120 g Powdered; 6) Botany Bay, 1 oz
    Category
    Food
    Distribution
    44 states
  • SevereNHTSA·18V265000·2018-04-25

    Lakota Recalls 2018-2019 Trailers Due to Ramp Detachment Risk

    Lakota is recalling 2018-2019 Bighorn, Charger, and Colt trailers because missing hardware may allow the rear ramp to detach while moving, increasing crash risk.

    Product
    LAKOTA — LAKOTA BIGHORN, CHARGER, COLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1411-2018·2018-04-25

    Philips Brilliance Big Bore CT Systems Recalled for Emergency Stop Defect

    Philips is recalling 119 Brilliance Big Bore CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient load or unload.

    Product
    Brilliance Big Bore (Radiology) - Model no. 728244, Computed Tomography X-Ray system Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1434-2018·2018-04-25

    Philips Panorama 1.0T MRI Recalled for Helium Gas Release Risk

    Philips is recalling Panorama 1.0T MRI scanners due to a potential risk of helium gas release into the examination room during a magnet quench.

    Product
    Panorama 1.0T, Model 781250 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1430-2018·2018-04-25

    Philips Multiva MRI Systems Recalled for Helium Gas Risk During Quench

    Philips is recalling 8,205 Multiva MRI systems worldwide due to a potential risk of helium gas release in the examination room during a magnet quench.

    Product
    Multiva systems, 1) Multiva 1.5T 8 R5 Model 781072, 2) Multiva 1.5T 16 R5 Model 781073, 3) Multiva 1.5T 8ch R5 based Model 781074, 4) Multiva 1.5T Model 781076, & 5) Multiva 1.5T 16ch R5 based Model 781078 Product Usage: Indicated for use as a diagnostic device. It can…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1382-2018·2018-04-25

    Draeger Infinity Acute Care System Recall for Alarm Failure

    Draeger Medical Systems is recalling Infinity Acute Care System monitoring solutions because invasive pressure alarms may not activate.

    Product
    Infinity Acute Care System (IACS) Monitoring Solution, Catalog Numbers: MS18841, MS20401, MS20407, MS20724, MS22956, MS25510, MS25520, MS25643, MS26196, MS26372, MS31818; UDI Information: 4049098054454, 4049098054447, 4049098054409, 4049098009799, 4049098009751…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1379-2018·2018-04-25

    Getinge Washer-Disinfector Accessory Recall for Potential Cart Unloading Hazard

    Getinge is recalling 170 automated loading/unloading accessories for Washer-Disinfector 86 Series units due to a risk of disinfected goods falling to the floor.

    Product
    Getinge AGS, FSLC, FSUC, RC accessory to Washer- Disinfector 86 Series UDI Info: 86 Series Washer Disinfector 07340153700246, 07340153700253, 07340153700260, 07340153700277 Getinge automated loading/unloading systems are intended to be used as an automatic…
    Category
    Medical Device
    Distribution
    Distributed nationwide