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.

Which agencies issued them

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.

44426–44450 of 79632

  • ModerateFDA (Devices)·Z-3212-2017·2017-10-04

    Teleflex Recalls LMA MADgic Devices Due to Labeling Deficiencies

    Teleflex Medical is recalling LMA MADgic devices because package labels may contain missing or incomplete information.

    Product
    LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c) MAD720 MADgic Intended for the application of topical anesthetics to the oropharynx and upper airway region
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1178-2017·2017-10-04

    Teva Recalls Acarbose Tablets Due to Incorrect Expiration Date Labeling

    Teva Pharmaceuticals USA is recalling 3,275 bottles of Acarbose Tablets, 25 mg, because the product labeling displays an incorrect expiration date of July 2018 instead of the correct date of July 2017.

    Product
    Acarbose Tablets, 25 mg, 100-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; NDC 16252-523-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3217-2017·2017-10-04

    Ultradent Paper Points Recalled Due to Sterile Barrier Labeling Error

    Ultradent Products, Inc. is recalling sterile Paper Points because the barcode label was placed underneath the sterile barrier and the product was re-wrapped.

    Product
    Ultradent Products, Inc. Paper Points, Size 45 PN #1558, 200 per container, sterile. Product Usage: The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins..
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3214-2017·2017-10-04

    Ultradent Paper Points Recalled for Sterile Barrier Labeling Error

    Ultradent Products is recalling sterile Paper Points because the barcode label was placed underneath the sterile barrier, compromising the product's sterile status.

    Product
    Ultradent Products, Inc. Paper Points, Size 20 PN #1560, 200 per container, sterile. Product Usage: The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3218-2017·2017-10-04

    Ultradent Paper Points Recalled Due to Sterile Barrier Labeling Error

    Ultradent Products is recalling sterile Paper Points because the barcode label was placed underneath the sterile barrier, compromising the product's sterility.

    Product
    Ultradent Products, Inc. Paper Points, Size 50 PN #1559, 200 per container, sterile. Product Usage: The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins..
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3215-2017·2017-10-04

    Ultradent Paper Points Recalled Due to Sterile Barrier Label Placement

    Ultradent Products is recalling sterile Paper Points because the barcode label was placed underneath the sterile barrier, potentially compromising sterility.

    Product
    Ultradent Products, Inc. Paper Points, Size 25 PN #1554, 200 per container, sterile. Product Usage: The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1179-2017·2017-10-04

    Sandoz Recalls Ampicillin Vials Due to Missing Labels

    Sandoz Inc is recalling 13,435 packs of Ampicillin for Injection because some vials are missing labels. The recall covers distribution in the USA and Puerto Rico.

    Product
    AMPICILLIN — AMPICILLIN (AMPICILLIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V616000·2017-10-03

    Braun Recalls 2016 BraunAbility MXV Vehicles Due to Airbag Sensor Defect

    Braun is recalling 2016 BraunAbility MXV wheelchair accessible vehicles because a seat position sensor may dislodge, potentially causing the frontal airbag to deploy with improper force.

    Product
    BRAUN — BRAUN BRAUNABILITY MXV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V615000·2017-10-03

    Great Dane Recalls 2018 Everest Trailers Due to Brake Caliper Bolt Issue

    Great Dane is recalling 2018 Everest trailers because brake caliper bolts may not be properly torqued, which could cause the caliper to detach and result in a loss of braking ability.

    Product
    GREAT DANE — GREAT DANE EVEREST SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18001·2017-10-03

    Playtex Recalls Children's Plates and Bowls Due to Choking Hazard

    Playtex is recalling approximately 3.6 million children's plates and bowls because the clear plastic layer can peel off, posing a choking hazard to young children.

    Product
    Children's Playtex plates and bowls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17E058000·2017-10-03

    UD Recalls One Hino Engine for 2008 UD1800 Trucks Due to Wear Risk

    UD Trucks is recalling one Hino engine sold as a replacement for 2008 UD1800 trucks because shifting wrist pin bushings may cause excessive cylinder wear and engine failure.

    Product
    UD — UD UD1800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E057000·2017-10-03

    NAPA and Evercraft 800lb Transmission Jacks Recalled for Bolt Failure

    International Specialty Services is recalling NAPA and Evercraft 800lb transmission jacks because a bolt may loosen, causing the saddle to destabilize and the transmission to tip over.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V614000·2017-10-02

    Trail King Recalls 2018 Fifth-Wheel Trailers Due to Brake Caliper Bolt Issue

    Trail King is recalling 2018 Fifth Wheel Live Bottom trailers because improperly torqued brake caliper bolts may allow the caliper to detach, increasing crash risk.

    Product
    TRAIL KING — TRAIL KING FIFTH-WHEEL LIVE BOTTOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E055000·2017-10-02

    IMMI Recalls School Bus Seats Due to Fracturing Buckle Mount Rods

    Indiana Mills and Manufacturing is recalling Generation IV school bus seats because the buckle mount rods may fracture, increasing injury risk in crashes.

    Product
    SEAT BELTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E056000·2017-10-02

    Hale Products Recalls Firefighting Water Pump Retaining Rings

    Hale Products is recalling retaining rings for firefighting water pumps that may corrode and fail, reducing water pressure and hindering firefighting efforts.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17T016000·2017-09-29

    Max-Trac Recalls Avon Viper Stryke Tires for Tread Separation Risk

    Max-Trac is recalling specific Avon Viper Stryke tires because a tread bulge or separation could cause loss of vehicle control and increase crash risk.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V608000·2017-09-29

    Kia Recalls 2014-2016 Soul Models Due to Steering Gear Separation Risk

    Kia is recalling 2014-2016 Soul and Soul EV vehicles because a pinion plug defect may allow the pinion gear to separate, potentially causing loss of steering and increasing crash risk.

    Product
    KIA — KIA SOUL, SOUL EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V609000·2017-09-29

    Mitsubishi Recalls Outlander and Lancer Models for Defective Starter Relays

    Mitsubishi is recalling 2015-2017 Outlander, Outlander Sport, Lancer, and Lancer Evolution vehicles because defective relays may cause engine stalls, reduced power, or overheating.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT, OUTLANDER, LANCER, LANCER EVOLUTION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V606000·2017-09-28

    Silver Eagle Vast-20W Trailer Brake Caliper Bolt Recall

    Silver Eagle is recalling 2018 Vast-20W converter dolly trailers because brake caliper bolts may not be properly torqued, risking caliper detachment and loss of braking ability.

    Product
    SILVER EAGLE — SILVER EAGLE VAST-20W
    Category
    Vehicle
    Distribution
    Distributed nationwide