The Recall Desk

State

Oklahoma product recalls

73,737 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,822
Critical
1,040
Severe
1,493
Most recent
2026-10-28

Of the 5,822 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 1,493 (26%) are Severe.

These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34126–34150 of 79559

  • HighNHTSA·19V749000·2019-10-18

    Collins Recalls 2018-2019 School Buses Lacking Rear Backup Cameras

    Collins Bus Corporation is recalling 2018-2019 TL400, TL408, TH400, and TH408 school buses that may lack rear backup cameras, increasing crash risk.

    Product
    COLLINS — COLLINS TL408, TH400, TH408, TL400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V743000·2019-10-18

    Subaru Recalls Impreza and Crosstrek for Electrical Software Defect

    Subaru is recalling 2017-2019 Impreza and 2018-2019 Crosstrek vehicles because a software defect may cause the engine to stall while driving, increasing crash risk.

    Product
    SUBARU — SUBARU IMPREZA, CROSSTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V751000·2019-10-18

    Vac-Tron Recalls 2015-2019 LP 873 SD Trailers Due to Sway Risk

    Vac-Tron is recalling 2015-2019 LP 873 SD heavy trailers because they may sway while being towed, increasing the risk of a crash.

    Product
    VAC-TRON — VAC-TRON LP 873 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V750000·2019-10-18

    Polaris Recalls 2015-2019 Slingshot Motorcycles for Electrical Fuse Defect

    Polaris is recalling 2015-2019 Slingshot motorcycles because excessive electrical current may damage battery fuse terminals, potentially causing loss of lighting or power steering and increasing crash risk.

    Product
    POLARIS — POLARIS SLINGSHOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V741000·2019-10-17

    Toyota Recalls Vehicles Due to Airbag Inflator Explosion Risk

    Toyota is recalling approximately 928,220 vehicles because previously replaced airbag inflators may explode due to propellant degradation, posing a risk of serious injury or death.

    Product
    SCION — SCION, LEXUS, TOYOTA XB, SC430, IS 250, IS 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V740000·2019-10-17

    Yetti Trailers Recalled for Missing Spindle Nut Retainer Clips

    Voyager Industries is recalling 2018-2020 Yetti trailers because missing retainer clips may allow spindle nuts to loosen, potentially causing the wheel to come off the axle.

    Product
    YETTI — YETTI TRAXX, GRAND ESCAPE, ANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E071000·2019-10-17

    Honda Recalls Rear Carriers for 2019-2020 Monkey Motorcycles

    Honda is recalling Genuine Accessory Rear Carriers for 2019-2020 Monkey motorcycles because they may fail under load, posing a crash risk.

    Product
    EQUIPMENT:MECHANICAL:CARRIER/RACK recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V745000·2019-10-17

    Subaru Recalls 2017 Impreza Vehicles Due to PCV Valve Defect

    Subaru is recalling 2017 Impreza vehicles because a defective PCV valve may break apart and enter the engine, causing a loss of power while driving.

    Product
    SUBARU — SUBARU IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V744000·2019-10-17

    Subaru Recalls Impreza and Crosstrek Vehicles for PCV Valve Defect

    Subaru is recalling 2017-2018 Impreza and 2018 Crosstrek vehicles because the PCV valve may break apart, potentially causing a loss of power while driving.

    Product
    SUBARU — SUBARU IMPREZA, CROSSTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0040-2020·2019-10-16

    Sara Lee Frozen Bakery Recalls Whole Grain Banana Muffins for Tree Nut Contamination

    Sara Lee Frozen Bakery is recalling Chef Pierre Small Whole Grain Banana Muffins after a consumer reported finding tree nut foreign material in the product.

    Product
    Chef Pierre ¿ SMALL WHOLE GRAIN BANANA MUFFINS NET WT 12 LB (5.44kg) 4 TRAYS/24/2 oz WHOLE GRAIN BANANA MUFFINS KEEP FROZEN CONTAINS WHEAT, EGGS DISTRIBUTED BY TYSON FOOD SERVICE SPRINGDALE, AR 72765-2020 UPC (01) 1 00 32100 08896 8
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0126-2020·2019-10-16

    Major Infants' Gas Relief Drops Recalled for Microbial Contamination

    GCP Laboratories is recalling Major Infants' Gas Relief Drops due to microbial contamination of the non-sterile product.

    Product
    Major Infants' Gas Relief Drops, Simethicone Oral Suspension USP, 1 FL OZ (30 mL) bottle, Distributed by: Major Pharmaceuticals 17177 N Laurel Park Drive, Suite 233 Livonia, MI 48152 USA. NDC 0904-5894-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0074-2020·2019-10-16

    BD FACSLyric Flow Cytometers Recalled for Potential False High Counts

    Becton, Dickinson and Company is recalling 22 BD FACSLyric Flow Cytometers because they may produce falsely high absolute counts when used with BD Trucount Tubes.

    Product
    BD FACSLyric Flow Cytometer, 3-Laser 12 Color Instrument, REF: 663029, when using BD Trucount Tubes
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Drugs)·D-0128-2020·2019-10-16

    Sandoz Recalls Ranitidine Capsules Due to NDMA Impurity Detection

    Sandoz is recalling 13,130 bottles of Ranitidine Hydrochloride Capsules 150mg because a trace amount of the impurity NDMA was detected.

    Product
    Sandoz Ranitidine Hydrochloride Capsules 150mg 500 Capsules Rx Only Manufactured by Sandoz Inc. Princeton, NJ 08540 Product of India NDC 0781-2855-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0127-2020·2019-10-16

    Sandoz Recalls Ranitidine Capsules Due to NDMA Impurity

    Sandoz is recalling specific lots of Ranitidine Hydrochloride Capsules 150mg because a trace amount of the impurity NDMA was detected.

    Product
    Sandoz Ranitidine Hydrochloride Capsules 150mg 60 Capsules Rx Only Manufactured by Sandoz Inc. Princeton, NJ Product of India NDC 0781-2855-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0130-2020·2019-10-16

    Morton Grove Recalls Prednisolone Sodium Phosphate Oral Solution Due to Impurity Failure

    Morton Grove Pharmaceuticals is recalling Prednisolone Sodium Phosphate Oral Solution because it failed impurity specifications for Prednisolone Impurity 14.

    Product
    Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, packaged in a 8 fl oz (237 mL) bottle, Rx only, Manufactured By Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053. NDC 60432-212-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V735000·2019-10-16

    Porsche Recalls Cayenne and Panamera for Brake Warning Defect

    Porsche is recalling 2017-2020 Cayenne and Panamera vehicles because the instrument cluster may fail to warn drivers when brake pads are worn out.

    Product
    PORSCHE — PORSCHE CAYENNE, PANAMERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0133-2020·2019-10-16

    DrKids Himasal Nasal Saline Recalled for Potential B. cepacia Contamination

    Unipharma is recalling DrKids Himasal Natural Nasal Saline Solution vials due to a precautionary measure regarding potential contamination with B. cepacia bacteria.

    Product
    DrKids Himasal Natural Nasal Saline Solution, packaged in Pre-measured Singe-Use Vials a) 0.5 mL Each (20 count) UPC 37030244608; b) 1.5 mL Each (20 count) UPC 370302446098, Manufactured in USA by: UNIPHARMA, LLC Tamarac, FL 33321
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V738000·2019-10-16

    BMW Recalls 2020 X3 and X4 Models for Steering Rack Defect

    BMW is recalling 2020 X3 M40i and X4 M40i vehicles because the steering rack pinion teeth may break, causing a loss of steering control.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0049-2020·2019-10-16

    Becton Dickinson Recalls CareFusion MaxPlus Clear Needleless Connectors

    Becton Dickinson is recalling 115,200 CareFusion MaxPlus Clear Needleless Connectors because the valve may fail to close, posing risks of blood loss and air embolism.

    Product
    CareFusion MaxPlus Clear Needleless Connector. Intended for Positive Displacement Connector for needleless access to the IV line and/or IV catheter during IV therapy Cat. No. MP1000-C
    Category
    Medical Device
    Distribution
    Distributed nationwide