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.

44201–44225 of 79632

  • HighFDA (Drugs)·D-0039-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Injection Bags Nationwide

    Pharmedium Services, LLC is voluntarily recalling 390 bags of compounded Oxytocin 20 units in Lactated Ringer's Injection due to subpotent drug levels.

    Product
    Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection USP in 1000 mL bag Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-241-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·17V690000·2017-11-01

    Heartland Recalls 2018 Pioneer Trailers Due to Propane Leak Risk

    Heartland is recalling 2018 Pioneer recreational trailers because the propane manifold block may be mounted too close to the shackle, creating a leak risk.

    Product
    HEARTLAND — HEARTLAND PIONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0050-2018·2017-11-01

    Nucletron Oncentra Brachy 4.5 Software Recalled for Incorrect Source Step Size

    Nucletron BV is recalling Oncentra Brachy 4.5 radiation therapy software because incorrect source step sizes may occur in treatment plans.

    Product
    Oncentra Brachy 4.5 radiation therapy software The firm name on the label is Nucletron B.V. Oncentra is a radiation therapy planning software designed to analyze and plan radiation treatments in three dimensions for the purpose of treating patients with cancer. The treatment…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0040-2018·2017-11-01

    Pharmedium Recalls Subpotent Oxytocin Lactated Ringer's Injection Bags

    Pharmedium Services, LLC is voluntarily recalling 978 bags of compounded Oxytocin in Lactated Ringer's Injection because the drug was subpotent.

    Product
    Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection USP in 1000 mL bag Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-241-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0045-2018·2017-11-01

    Sysmex Fluorocell PLT Reagent Recalled for Potential Inaccurate Platelet Results

    Sysmex America is recalling Fluorocell PLT reagent lots because they may produce falsely low platelet results, potentially affecting diagnostic accuracy.

    Product
    Sysmex Fluorocell(R) PLT Fluorocell PLT is used to stain platelets in a diluted blood sample for the counting of platelets with the Sysmex XN-Series automated hematology analyzers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0042-2018·2017-11-01

    Encore Medical Recalls EMPOWR PS Knee Inserts Due to Packaging Error

    Encore Medical is recalling 46 EMPOWR PS Knee Inserts because one unit was packaged with the wrong implant. The recall covers US nationwide distribution.

    Product
    EMPOWR PS KNEE(TM) e+, REF 343-19-707, SIZE 7, 19mm, QTY 01, GREY, STERILE Product Usage The EMPOWR PS Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0041-2018·2017-11-01

    Encore Medical Recalls EMPOWR PS Knee Inserts Due to Packaging Error

    Encore Medical is recalling 48 units of EMPOWR PS Knee inserts because one unit was packaged with the wrong implant reference number.

    Product
    EMPOWR PS KNEE(TM) e+, REF 343-13-708, SIZE 8, 13mm, QTY 01, SKY BLUE, STERILE Product Usage The EMPOWR PS Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0051-2018·2017-11-01

    Wockhardt Recalls Enalapril Maleate Tablets Due to Impurity Failures

    Wockhardt USA is recalling 5mg Enalapril Maleate tablets because they failed impurity specifications. The recall covers 5,050 bottles distributed nationwide.

    Product
    Enalapril Maleate tablets, USP, 5mg, 1000-count bottles, Rx only, Manufactured by: Wockhardt Limited H-14/2, M.I.D.C. Area, Waluj, Aurangabad, Maharashtra, India, Distributed by: Wockhardt, USA LLC, 20 Waterview Blvd, Parsippany, NJ 07054, USA. NDC: 64679-924-03;
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0052-2018·2017-11-01

    Teva Recalls Methylphenidate Hydrochloride Tablets Due to Dissolution Failures

    Teva Pharmaceuticals USA is recalling 58,292 bottles of Methylphenidate Hydrochloride Tablets USP, 20 mg, because they failed to meet dissolution specifications.

    Product
    Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA, NDC 0591-5884-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0073-2018·2017-11-01

    Vi-Jon Recalls Equate and Studio 35 Face Moisturizers for Stability Failures

    Vi-Jon, Inc. is recalling Equate and Studio 35 Clarifying Face Daily Moisturizers because the products failed stability specifications. The recall covers 67,532 bottles distributed nationwide.

    Product
    Equate Beauty Clarifying Face Daily Moisturizer 4 fl. oz. (118 mL) Distributed by: Wal-Mart Stores, Inc. Bentonville, AR 72716, NDC # 4903594126 UPC # 681131150774. Studio 35 Beauty Daily Clarifying Face Daily Moisturizer 4 fl. oz. (118 mL) Distributed By: Walgreen Co. 200…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0146-2018·2017-11-01

    Taro Recalls Fluocinonide Gel Due to Dapsone Cross-Contamination

    Taro Pharmaceuticals is recalling 16,944 tubes of Fluocinonide Gel USP 0.05% because traces of Dapsone were found in the finished product.

    Product
    FLUOCINONIDE — FLUOCINONIDE (FLUOCINONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V686000·2017-10-30

    Mitsubishi Mirage Recall: Air Bags May Fail to Deploy in Crash

    Mitsubishi is recalling 2014-2018 Mirage vehicles because the air bag system may disable itself due to sensor errors, increasing injury risk.

    Product
    MITSUBISHI — MITSUBISHI MIRAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V683000·2017-10-30

    BMW Recalls 740,561 Vehicles for PCV Valve Fire Risk

    BMW is recalling 740,561 vehicles from 2007-2011 because a short circuit in the PCV valve heater can cause a fire.

    Product
    BMW — BMW 328I, 128I, X5, 530I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18018·2017-10-30

    Polaris Recalls General Off-Highway Vehicles Due to Steering Shaft Hazard

    Polaris is recalling about 19,000 General side-by-side vehicles because the steering wheel shaft can shift and detach, creating a crash risk.

    Product
    Polaris General side-by-side recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V687000·2017-10-30

    MCI Recalls 2018 J4500 Buses Due to Incorrect Air Line Connections

    Motor Coach Industries is recalling 2018 MCI J4500 buses because air lines were incorrectly hooked to pressure gauges, potentially delaying driver response to low air conditions.

    Product
    MCI — MCI J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V685000·2017-10-27

    Eldorado Buses Recalled for Stuck Seat Belt Buckles

    Eldorado is recalling 2017 Axess, Arrivo, XHF, and E-Z Rider II buses because seat belt buckles may be stuck, preventing use.

    Product
    ELDORADO — ELDORADO AXESS, ARRIVO, XHF, E-Z RIDER II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V682000·2017-10-27

    Indian Recalls 2017-2018 Motorcycles for Non-Compliant Headlight Assemblies

    Indian Motorcycle is recalling 2,096 models from 2017-2018 because some may have European-market headlights that fail US safety standards, increasing crash risk.

    Product
    INDIAN — INDIAN CHIEFTAIN DARK HORSE, CHIEFTAIN, CHIEF VINTAGE, SPRINGFIELD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V680000·2017-10-26

    Tremcar Recalls Hutchinson and Tremcar Trailers Due to Weak Rear Impact Guards

    Tremcar is recalling specific Hutchinson and Tremcar trailers because their rear impact guards were made with insufficiently strong aluminum alloy.

    Product
    HUTCHINSON — HUTCHINSON, TREMCAR 406 2 AXLE SEMI-TRAILER, 406 B-TRAIN PUP, 406 QUAD WAGON, 406 3 AXLE SEMI-TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V677000·2017-10-26

    Forest River Recalls 2017-2018 Rockwood and Flagstaff Travel Trailers

    Forest River is recalling 2017-2018 Rockwood and Flagstaff travel trailers because the slide room arm may damage the rear tire, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide