The Recall Desk

State

Oklahoma product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38701–38725 of 79563

  • SevereNHTSA·18V848000·2018-11-28

    Honda Recalls 2019 Ridgeline and Pilot for Air Bag Deployment Risk

    Honda is recalling 2019 Ridgeline and Pilot vehicles because a trim panel clip may interfere with right-side curtain air bag deployment in a crash.

    Product
    HONDA — HONDA RIDGELINE, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0475-2019·2018-11-28

    Tosoh AIA-2000 Analyzer Recall Due to Potential Wash Solution Defect

    Tosoh Bioscience is recalling seven AIA-2000 analyzers because a liquid suction pump defect may cause incomplete washing, leading to inaccurate test results.

    Product
    AIA-2000 Analyzer, Model Nos. AIA-2000LA, AIA-2000ST - Product Usage: The AIA-2000 is capable of performing three methods of immunoassay: an immunoenzymetric (IEMA) or sandwich immunoassay, a competitive binding (EIA) immunoassay, and a two-step immunoenzymetric immunoassay. An…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0482-2019·2018-11-28

    GE Healthcare Recalls Panda iRes Infant Radiant Warmers Due to Electric Leakage

    GE Healthcare is recalling 1,724 Panda iRes Infant Radiant Warmers worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Panda iRes Infant Radiant Warmer. Device sold under the following product names: Panda iRes Warmer and Panda iRes Bedded Warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0483-2019·2018-11-28

    GE Healthcare Recalls Panda Freestanding Infant Warmers Due to Electric Leakage

    GE Healthcare is recalling 1,724 Panda Freestanding Infant Warmers worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Panda Freestanding Warmer. Device sold under the following product names: Panda Freestanding Warmer and Panda Freestanding Warmer Generic ATO Model. Infant Radiant warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V844000·2018-11-28

    Porsche Recalls 2017-2018 Models Due to Ski Bag Strap Defect

    Porsche is recalling certain 2017-2018 Cayenne and Macan vehicles because the optional ski bag strap may tear, increasing injury risk in a crash.

    Product
    PORSCHE — PORSCHE CAYENNE, MACAN, MACAN GTS, MACAN S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0266-2019·2018-11-28

    L. Perrigo Recalls Calcium Carbonate Antacid Tablets Due to Metal Particles

    L. Perrigo is recalling specific lots of calcium carbonate antacid tablets because they were found to contain metal particles.

    Product
    Antacid Tablets, Calcium Carbonate chewable tablets, 750mg, 60-count bottle, OTC, [Healthy Accents brand NDC: 55316-014-72, Distributed by DZA Brands, LLC, Salisbury, NC 28147, Scarborough, ME 04074], [HealthMart Pharmacy brand NDC: 62011-0295-1, Distributed by McKessen, One…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0481-2019·2018-11-28

    GE Healthcare Recalls Giraffe Infant Warmers Due to Electric Leakage Risk

    GE Healthcare is recalling 1,724 Giraffe infant radiant warmers worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Giraffe Warmer. Device sold under the following product names: Giraffe Warmer and Giraffe Bedded Warmer. infant radiant warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0480-2019·2018-11-28

    GE Healthcare Recalls Giraffe Incubator Carestations Due to Electric Leakage

    GE Healthcare is recalling 1,724 Giraffe Incubator Carestations worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Giraffe Incubator Carestation. Neonatal incubator. Device sold under the following product names: Carestation and Carestation CS1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0479-2019·2018-11-28

    GE Healthcare Recalls Giraffe OmniBed Neonatal Incubators Due to Electric Leakage

    GE Healthcare is recalling 1,724 Giraffe OmniBed Carestation neonatal incubators worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Giraffe OmniBed Carestation. Neonatal incubator. Device sold under the following product names: Carestation and Carestation CS1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0489-2019·2018-11-28

    Merck Minicon Clinical Sample Concentrators Recalled for Performance Issues

    Merck Millipore is recalling Minicon Clinical Sample Concentrators because they may take up to 24 hours to concentrate samples, delaying diagnostic tests.

    Product
    Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon CS-15) Minicon concentrators are non-sterile, disposable, multiwall ultrafiltration devices. Minicon¿ clinical sample concentrators are for in vitro diagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0476-2019·2018-11-28

    Ortho-Clinical VITROS dLDL Reagent Recalled for Negatively Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products dLDL Reagent GENs 26 and 27 because the in vitro diagnostic may produce negatively biased results.

    Product
    VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Diagnostic to quantitatively measure LDL Cholesterol (LDLC) Product Code: 6801728 UDI (10758750006793)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0283-2019·2018-11-28

    Dr. Reddy's Recalls Clopidogrel Tablets Due to Dissolution Failure

    Dr. Reddy's Laboratories is recalling specific lots of Clopidogrel Bisulfate tablets because they failed dissolution testing during stability checks.

    Product
    CLOPIDOGREL BISULFATE — CLOPIDOGREL BISULFATE (CLOPIDOGREL BISULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0275-2019·2018-11-28

    Ecolab Recalls Medi-Stat Foam Hand Soap Due to Labeling Error

    Ecolab Inc is recalling 14,108 bottles of Medi-Stat Foam Antimicrobial Hand Soap because the label may not match the formula in the bottle.

    Product
    Medi-Stat Foam, Antimicrobial Hand Soap, Chloroxylenol 0.5%, 1250 mL (42.3 fl oz), OTC, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102, NDC 47593-503-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0388-2019·2018-11-28

    GE Healthcare Recalls DeltaVision OMX SR Imaging Systems Due to Interlock Defect

    GE Healthcare Biosciences is recalling 39 DeltaVision OMX SR Imaging Systems because the safety interlocks are not wired to be single-fault tolerant.

    Product
    DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision OMX SR Imaging System is a piece of laboratory equipment for super resolution imaging offluorescently-la beling biological samples. Techniques such as 3D Structured Illumination, Total Internal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0273-2019·2018-11-28

    Nitrofurantoin Capsules Recalled for Potential Cross-Contamination with Unrelated Ingredients

    American Health Packaging is recalling specific lots of Nitrofurantoin Capsules due to potential cross-contamination with unrelated active ingredients.

    Product
    Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals), 100 mg, 100-count Unit Dose Blisters, Rx only, Amerisource Health Services DBA American Health Packaging, 2550-A John Glenn Avenue Columbus, OH 43217, NDC 68084-446-01 (Individual Dose NDC: 68064-446-11)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V836000·2018-11-27

    Audi Recalls A5 and A4 Allroad for Passenger Air Bag Defect

    Volkswagen Group of America is recalling 2018 Audi A5 Sportback and 2017-2018 Audi A4 Allroad vehicles because a passenger air bag mounting screw may not be sufficiently tightened.

    Product
    AUDI — AUDI A5, A4 ALLROAD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V839000·2018-11-27

    Mercedes-Benz Recalls 2019 Models for Seat Belt Pre-Tensioner Defect

    Mercedes-Benz is recalling 4,969 2019 vehicles because seat belt pre-tensioners may not activate in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH E 450, S 450, C 300, S 560 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V840000·2018-11-27

    Mercedes-Benz Recalls 2019 GLC 300 for Steering Assist Failure

    Mercedes-Benz is recalling 2019 GLC 300 vehicles because a steering sensor may fail, deactivating power assist and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V833000·2018-11-27

    Lamborghini Recalls Gallardo Vehicles Due to Software Warning Failure

    Lamborghini is recalling 2011-2014 Gallardo vehicles because engine software may erase trouble codes, preventing warning lamps from illuminating for safety system failures.

    Product
    LAMBORGHINI — LAMBORGHINI GALLARDO
    Category
    Vehicle
    Distribution
    Distributed nationwide