The Recall Desk

State

Oklahoma product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49876–49900 of 79640

  • ModerateFDA (Devices)·Z-0128-2017·2016-10-26

    BD Biosciences Recalls Contaminated CD79b PE Antibody Reagent

    Becton, Dickinson and Company is recalling 14 units of CD79b PE antibody reagent due to contamination with a FITC conjugate of unknown specificity.

    Product
    CD79b PE (ASR) , Catalog number 335816 ; Hematology: The CD79b antibody recognizes an epitope on the extracellular domain of a 3640 kilodalton (kDa) type I membrane glycoprotein. Immunoglobulin (Ig) antigen receptors are composed of a non-covalently associated complex of Ig…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0130-2017·2016-10-26

    ConMed Recalls CORE Suction Irrigation Handpieces Due to Packaging Seal Defects

    ConMed Corporation is recalling CORE Suction Irrigation Handpieces because packaging seal creases may compromise sterility. The recall covers units distributed in the US and internationally.

    Product
    CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe for Single Solution or Dual Bags, Catalog Number CD8190 The CORE Trumpet (CD81XX, CD83XX, and CD84XX) has applications in gynecological laparoscopy, laparoscopic cholecystectomy and other laparoscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0089-2017·2016-10-26

    Ortho VITROS Chemistry GLU Slides Recalled for Potential Assay Interference

    Ortho-Clinical Diagnostics is recalling VITROS GLU Slides because certain substances, including N-Acetylcysteine, may interfere with glucose measurements.

    Product
    VITROS Chemistry Products GLU Slides, REF/Product Code 170 7801 (300 slides per sales unit), Unique Device Identifier No. 10758750009572, Rx ONLY, IVD --- For in vitro diagnostic use only. VITROS Chemistry Products GLU Slides quantitatively measure glucose (GLU)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0226-2017·2016-10-26

    Hillcrest Farms Poultry Gravy Mix Recalled for Lead Contamination

    National Foods Packaging Inc is recalling Hillcrest Farms Poultry Gravy Mix because a spice ingredient was found to contain elevated levels of lead.

    Product
    Hillcrest Farms Poultry Gravy Mix in 25lb brown poly-lined bags
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0093-2017·2016-10-26

    Tearscience Recalls LipiFlow Thermal Pulsation System Activators Due to Error Condition

    Tearscience, Inc. is recalling 1,200 LipiFlow Thermal Pulsation System Activators because the device may automatically stop treatment during patient use.

    Product
    LipiFlow thermal Pulsation System, consisting of Console and Activator, Model LFD-1100 The LipiFlow Thermal Pulsation System is intended for use by physicians as a prescription device for the application of localized heat and pressure therapy in adult patients with chronic…
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Food)·F-0165-2017·2016-10-26

    Entenmann's Little Bites Variety Recalled Due to Plastic Presence

    BIMBO Bakeries USA Inc. is recalling 45,600 boxes of Entenmann's Little Bites Variety due to the presence of plastic in the muffins and brownies.

    Product
    Entenmann's Little Bites Variety - 20 pouches labeled for resale 10 Chocolate Chip; 5 Blueberry; 5 Fudge Brownie; Net Wt 2 lbs.; Distributed by: Entenmann's Inc., General Offices, PO #976, Horsham, PA 19044. Best by: September 24, 2016/ 3098; UPC:7203001799
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0111-2017·2016-10-26

    Teva Recalls Paricalcitol Capsules Due to Impurity Test Failures

    Teva Pharmaceuticals is recalling specific lots of Paricalcitol Capsules because stability testing revealed out-of-specification impurities.

    Product
    PARICALCITOL Capsules, 4 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD 21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-7658-56.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0110-2017·2016-10-26

    Teva Recalls Paricalcitol Capsules Due to Impurity Test Failures

    Teva Pharmaceuticals is recalling 5,556 bottles of Paricalcitol Capsules because stability testing revealed out-of-specification impurities.

    Product
    PARICALCITOL Capsules, 2 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD 21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-7657-56.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0109-2017·2016-10-26

    Teva Recalls Paricalcitol Capsules Due to Impurity Test Failures

    Teva Pharmaceuticals is recalling 32,015 bottles of Paricalcitol Capsules, 1 mcg, because stability testing revealed out-of-specification impurities.

    Product
    PARICALCITOL Capsules, 1 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD 21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-7656-56.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E079000·2016-10-25

    Atwood Recalls Left Side Seat Adjusters for Crash Safety Non-Compliance

    Atwood Mobile Products is recalling specific left side seat adjusters used in vehicle seat belts because they may allow seats to move during a crash, increasing injury risk.

    Product
    SEAT BELTS:FRONT:ANCHORAGE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·100-2016·2016-10-25

    Crider Recalls Canned Organic Roasted Chicken Breast Due to Foreign Matter

    Crider Inc. is recalling approximately 5,610 pounds of canned Organic Roasted Chicken Breast due to possible foreign matter contamination.

    Product
    Crider, Inc. — Crider Inc. Recalls Canned Organic Roasted Chicken Breast Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16E080000·2016-10-25

    Ivolution Recalls JX-SKY Helmets Due to Crash Safety Non-Compliance

    Ivolution Sports is recalling specific JX-SKY helmets because a metal screw prevents a detachable feature from releasing during a crash, increasing neck injury risk.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V772000·2016-10-24

    Jayco Recalls 2017 Eagle Fifth Wheel Trailers for Axle Defect

    Jayco is recalling specific 2017 Eagle fifth wheel trailers due to axles with insufficient load capacity, which may lead to tire failure and increased crash risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V769000·2016-10-24

    ARBOC Spirit of Liberty Recall for Engine Run Lockout Wiring Defect

    ARBOC is recalling 2016 Spirit of Liberty vehicles because improper wiring may allow the engine to start while a mechanic is working on it, posing a risk of injury or death.

    Product
    ARBOC — ARBOC SPIRIT OF LIBERTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V775000·2016-10-24

    Toyota Recalls 2016 Highlanders Due to Brake Fluid Sensor Wiring Issue

    Toyota is recalling 7,056 model year 2016 Highlanders because the brake fluid level sensor may not be connected to the wire harness, potentially decreasing braking performance.

    Product
    TOYOTA — TOYOTA HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V765000·2016-10-21

    Navistar Recalls School Buses with Defective Wheelchair Lifts

    Navistar is recalling certain 2015-2017 IC Bus school buses equipped with specific Ricon wheelchair lifts. The defect may cause the lift platform to fall out of the vehicle, increasing injury risk.

    Product
    IC BUS — IC BUS CESB, RESB, CASB, AE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V764000·2016-10-21

    Kaufman Recalls 2015-2016 Mini Car Haulers Due to Spring Defect

    Kaufman is recalling 2015-2016 Mini Car Haulers because a spring eye may break, allowing the axle to slide and potentially causing a crash.

    Product
    KAUFMAN — KAUFMAN MINI CAR HAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V766000·2016-10-21

    Navistar Recalls 2016 IC Bus RECB Models Due to Wheelchair Lift Defect

    Navistar is recalling 2016 IC Bus RECB transit buses equipped with specific Ricon wheelchair lifts. Defective pivot holes may allow bearings to shift, causing the lift platform to fall and injure operators.

    Product
    IC BUS — IC BUS RECB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V768000·2016-10-21

    Newmar Recalls 2017 Motorhomes Due to Hydraulic Step Retraction Risk

    Newmar is recalling 2017 King Aire, Essex, and London Aire motorhomes because the hydraulic entry step controller may allow steps to retract unexpectedly, increasing the risk of injury.

    Product
    NEWMAR — NEWMAR LONDON AIRE, KING AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·098-2016·2016-10-21

    Brookwood Farms Recalls Pulled Pork Due To Undeclared Soy Allergen

    Brookwood Farms is recalling 126,570 pounds of pulled pork products because they contain soy, an undeclared allergen. No illnesses have been reported.

    Product
    Brookwood Farms — Brookwood Farms, Inc. Recalls Pulled Pork Products Due To Misbranding And An Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide