The Recall Desk

State

Oklahoma product recalls

73,833 recalls have nationwide distribution and so reach Oklahoma. 5,824 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,824
Critical
1,040
Severe
1,494
Most recent
2026-11-14

Of the 5,824 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 5,824 recalls whose distribution notice names Oklahoma specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58301–58325 of 79657

  • ModerateUSDA FSIS·093-2015·2015-06-17

    Pinnacle Foods Recalls Swanson Turkey Dinners for Undeclared MSG

    Pinnacle Foods is recalling approximately 668,316 pounds of Swanson Stuffing Baked Turkey dinners because the product contains monosodium glutamate (MSG) that is not declared on the label.

    Product
    Recall Notification Report 093-2015 (Poultry Products )
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2411-2015·2015-06-17

    Nuevotanicals Recalls K SHOT Kratom Supplement Due to Kratom Content

    Nuevotanicals is recalling K SHOT botanical supplement shots because the products contain Kratom. The recall affects 10,000 units distributed across 12 states.

    Product
    K SHOT 0.5 fl. oz (15 ml) 9 GRAMS OF HIGH QUALITY KRATOM LEAF PER BOTTLE Botanical Supplement Shot 100% Natural PURE ALKALOID CONCENTRATE OIL 100% NATURAL Vegan, Kosher, Halal, and Ital friendly
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Food)·F-2415-2015·2015-06-17

    FDA Recalls Unlabeled Green Malay Kratom Bulk Product

    The FDA is recalling 77 kg of unlabeled Green Malay Kratom bulk product in 1-gallon jugs due to the presence of Kratom.

    Product
    Green Malay/MD bulk in 1 gallon plastic jugs, no product label
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-1746-2015·2015-06-17

    Becton Dickinson Recalls BBL Port A Cul Tubes Due to Oxidation

    Becton Dickinson is recalling BBL Port A Cul tubes because excessive oxidation may affect the viability of anaerobic microorganisms.

    Product
    BBL Port A Cul tubes, catalog number 221606. Patient sample collection tubes. BBL Port A Cul tubes, jars and vials contain a reduced transport medium and are intended to maintain the viability of anaerobic, facultative and aerobic microorganisms during transport from the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2416-2015·2015-06-17

    Nuevotanicals Recalls Unlabeled Kratom Powder in Freezer Bags

    Nuevotanicals is recalling 326 kg of unlabeled Kratom powder in 500 g freezer bags distributed to 12 states.

    Product
    Max powder in Ziploc-type freezer bags in 500 g increments, no product label
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Food)·F-2405-2015·2015-06-17

    Rugby Poly Vitamin Liquid Recalled for Packaging Label Mismatch

    Pharmatech LLC is recalling Rugby Poly Vitamin Liquid, 50ml, because the outside packaging may have incorrect lot, expiration, or product identity information.

    Product
    Rugby Poly Vitamin Liquid, 50ml
    Category
    Drug
    Distribution
    37 states
  • ModerateFDA (Devices)·Z-1720-2015·2015-06-17

    Roscoe Mini Neb Compressor User Manual Recall for Warning Updates

    Compass Health Brands is recalling 219,353 Roscoe Mini Neb Compressor user manuals to add warnings about proper handling and storage to reduce power cord damage.

    Product
    Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage: Inhaler therapy that converts liquid medicine into a fine mist that is easily inhaled.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1754-2015·2015-06-17

    Biomet Recalls Hip Components Due to Incorrect GTIN Labeling Codes

    Biomet is recalling specific hip joint replacement components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.

    Product
    Mallory/Head Primary Hip System; Size 11, 160 mm, Lateralized Femoral Stem; Ti-6Al-4V; Porous Plasma Uncemented, & Mallory/Head Total Hip System Size 12, 165 mm, Bi- Metric Femoral Components. Hip joint replacement components include: femoral stems, femoral heads, acetabular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1755-2015·2015-06-17

    Biomet Shoulder Joint Replacement Components Recalled for Incorrect GTIN Codes

    Biomet, Inc. is recalling specific shoulder joint replacement components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.

    Product
    Comprehensive Shoulder System, 4 mm, 122 mm long, Primary Shoulder Stem, Ti-6Al-4V, Standard Length Porous Plasma. Shoulder joint replacement components include humeral stems, humeral heads, and glenoid components.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1756-2015·2015-06-17

    Biomet Knee Joint Replacement Components Recalled for Incorrect GTIN Codes

    Biomet is recalling MCK Maximum Congruent Knee System components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.

    Product
    MCK Maximum Congruent Knee System, BIOMET FINNED PRI STEM 40MM; 80 x 10MM; 80 x 12.5 MM; 80 x 15 MM Knee joint replacement prostheses components include femoral, tibial, and patellar components.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1757-2015·2015-06-17

    Biomet Recalls Hip Joint Components Due to Incorrect GTIN Labeling

    Biomet is recalling 1,315 hip joint replacement components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.

    Product
    Biomet Cobalt-Chrome Femoral Components, 32MM MOD HEAD COCR -6MM NECK; 32MM MOD HEAD COCR -3 MM NECK; 32MM MOD HEAD COCR STD NECK ; 32MM MOD HEAD COCR +3MM NECK; 32MM COCR MOD HD +6MM NO SKIRT Hip joint replacement components include: femoral stems, femoral heads, acetabular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V376000·2015-06-16

    EverGreen Recalls 2015 Travel Trailers Due to Wheel Stud Defect

    EverGreen is recalling 2015 i-Go, Ever-Lite, Sun Valley, and Ascend travel trailers because wheel studs may break, potentially causing the wheel to detach.

    Product
    EVERGREEN — EVERGREEN EVER-LITE, I-GO, ASCEND, SUN VALLEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V378000·2015-06-16

    Great Dane Recalls 2015 Converter Dollies Due to Brake Valve Defect

    Great Dane is recalling 111 model year 2015 Converter Dolly trailers because a brake valve defect may cause brake drag, leading to overheating, fire, or wheel detachment.

    Product
    GREAT DANE — GREAT DANE CONVERTER DOLLY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V379000·2015-06-16

    Vactor and Guzzler Vacuum Trucks Recalled for Boiler Assembly Defect

    Vactor is recalling 2014-2015 HXX and 2100 Plus trucks, and Guzzler Guzzcavator trucks, because incorrect boiler assembly hardware may cause the unit to detach, increasing crash risk.

    Product
    GUZZLER — GUZZLER, VACTOR GUZZCAVATOR, 2100 PLUS, HXX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15165·2015-06-16

    Bunnies by the Bay Recalls Pull Toys Due to Choking Hazard

    Bunnies by the Bay is recalling Bud and Skipit Wheely Cute Pull Toys because wheel hub caps can break off, posing a choking hazard to young children.

    Product
    Bud and Skipit Wheely Cute Pull Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V377000·2015-06-16

    EverGreen Recalls Fifth Wheel Trailers Due to Step Rivet Failure Risk

    EverGreen is recalling 2014-2016 fifth wheel trailers because a rivet on the entry steps may shear, causing the steps to give and increasing the risk of injury.

    Product
    EVERGREEN — EVERGREEN LIFESTYLE, ALPHA GOLD, BAY HILL, TESLA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V370000·2015-06-15

    Honda Recalls Vehicles for Passenger Air Bag Inflator Rupture Risk

    Honda is recalling specific 2001-2007 models because the passenger air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    HONDA — HONDA, ACURA CIVIC, ACCORD, CIVIC GX, CIVIC HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V375000·2015-06-15

    Newmar Recalls 2015 King Aire and Essex for Suspension Defect

    Newmar is recalling 2015 King Aire and Essex vehicles because tag axle suspension hangers may move, increasing crash risk.

    Product
    NEWMAR — NEWMAR KING AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V373000·2015-06-15

    Volkswagen Recalls 2015 Passat Vehicles for Brake Line Tightening Issue

    Volkswagen is recalling 2015 Passat vehicles because a brake line may not be properly tightened, potentially causing fluid leaks and reduced braking performance.

    Product
    VOLKSWAGEN — VOLKSWAGEN PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V374000·2015-06-15

    New Horizons Recalls 2013-2015 Summit and Majestic RVs for Step Defect

    New Horizons is recalling 2013-2015 Summit and Majestic RVs because a rivet on the quad entry steps may fail, causing the steps to give and increasing the risk of injury.

    Product
    NEW HORIZONS — NEW HORIZONS SUMMIT, MAJESTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E051000·2015-06-15

    Alcoa Recalls 22.5-Inch Aluminum Wheels Due to Forging Defect

    Alcoa is recalling specific 22.5-inch aluminum wheels manufactured in April and May 2015 because a forging defect may cause the rim flange to separate during tire mounting.

    Product
    WHEELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide