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.

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.

45351–45375 of 79632

  • HighFDA (Devices)·Z-2763-2017·2017-08-02

    Fisher Diagnostics Recalls FDP Latex Reagent Due to Reduced Sensitivity

    Fisher Diagnostics is recalling specific lots of Pacific Hemostasis FDP Latex Reagent because reduced sensitivity may cause false negative test results.

    Product
    Pacific Hemostasis FDP Latex Reagent, REF/Model Number 100651, UDI 00845275000870, 1 x 5 mL, IVD; --- Fisher Diagnostics, a division of Fisher Scientific Company, LLC, a part of Thermo Fisher Scientific Inc., Middletown, VA 22645-1905 USA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2767-2017·2017-08-02

    Medtronic Recalls DLP Pressure Monitoring Extension Line Adapters

    Medtronic Perfusion Systems is recalling DLP Pressure Monitoring Extension Line Adapters due to small pinholes in sterile packaging.

    Product
    DLP Pressure Monitoring Extension Line Adapters Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmonary bypass surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2888-2017·2017-08-02

    BioHealth Pasture Fed Protein Recalled for Undeclared Wheat

    Innovative Nutrition Technologies is recalling BioHealth Pasture Fed Precision Blend Time Release Protein in Cookies and Cream flavor because the product contains undeclared wheat.

    Product
    BioHealth Pasture Fed Precision Blend Time Release Protein: Cookies and Cream Flavor; Sold in 2 lb.(960G) UPC 6 42014 59446 7 and 4 lb. (1,920G) UPC 6 42014 59447 4 white plastic containers.
    Category
    Food
    Distribution
    17 states
  • ModerateFDA (Devices)·Z-2765-2017·2017-08-02

    Medtronic DLP Antegrade/Retrograde Adapter Recalled for Packaging Pinholes

    Medtronic is recalling DLP Antegrade/Retrograde Adapters because small pinholes were found in a single packaging configuration of sterile pouches.

    Product
    DLP Antegrade/Retrograde Adapter Method for perfusion of cardioplegia alternately in either an antegrade or retrograde fashion. It is fitted with flexible lines and standard luer sites to facilitate direct connections to the cannulae
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2768-2017·2017-08-02

    Medtronic Recalls DLP Pressure Display Sets Due to Packaging Pinholes

    Medtronic Perfusion Systems is recalling DLP Pressure Disposable Pressure Display Sets because small pinholes were found in the sterile packaging.

    Product
    DLP Pressure Disposable Pressure Display Sets Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmonary bypass surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2761-2017·2017-08-02

    Atrium iCAST and Advanta V12 Stents Recalled for Incorrect Hub Labeling

    Atrium Medical Corporation is recalling specific iCAST and Advanta V12 covered stents because the catheter hub was printed with incorrect dimensional information.

    Product
    Atrium iCAST Balloon Expandable Covered Stent; 7mm x 22mm x 120cm; Model/Part Number 85455 (Marketed in U.S. only) Atrium Advanta V12 Balloon Expandable Covered Stent; 7mm x 22mm x 120cm; Model/Part Number 85355 (Marketed OUTSIDE U.S. only) The iCAST Covered Stent is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2766-2017·2017-08-02

    Medtronic Recalls DLP Cardioplegia Adapters Due to Packaging Pinholes

    Medtronic Perfusion Systems is recalling DLP Cardioplegia Adapters with Pressure Port because small pinholes were identified in a single packaging configuration of sterile pouches.

    Product
    DLP Cardioplegia Adapter with Pressure Port Provides access for a pressure monitoring needle near the connection to the cardioplegia cannula. These adapters are intended for use in conjunction with the delivery of cardioplegia solution and to provide access for pressure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2757-2017·2017-08-02

    Cardinal Health Recalls Mislabeled Sterile Surgical Drapes

    Cardinal Health is recalling specific lots of sterile surgical drapes because the outer labels do not match the packaged product inside.

    Product
    Converters(R) Under Buttocks Drape with Fluid Control Pouch II, REF 8482, STERILE R, Qty. 1, Cardinal Health, Waukegan, IL A surgical drape and drape accessories is a device made of natural or synthetic materials intended to be used as a protective patient covering, such as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2758-2017·2017-08-02

    Cardinal Health Recalls Tiburon Arthroscopy Drapes Due to Labeling Mismatch

    Cardinal Health is recalling specific lots of Tiburon Arthroscopy Drapes because the outer labels do not match the packaged product.

    Product
    Converters(R) Tiburon(R) Arthroscopy Drape, REF 9414, STERILE EO, Qty. 1, Cardinal Health, Waukegan, IL A surgical drape and drape accessories is a device made of natural or synthetic materials intended to be used as a protective patient covering, such as to isolate a site of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E042000·2017-08-01

    Timken Recalls Rear Hub Unit Bearings for Ford Explorers

    Timken is recalling specific rear hub unit bearings for 2011-2017 Ford Explorer 4X2 vehicles because they lack a self-retention feature, which could cause the wheel to separate.

    Product
    SUSPENSION:REAR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V483000·2017-08-01

    Utility VS2RA Trailer Recall for Detaching Mud Flap Bracket

    Utility Trailer is recalling 2017 VS2RA trailers because a weld defect may allow the mud flap bracket to detach, creating a road hazard.

    Product
    UTILITY — UTILITY VS2RA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E040000·2017-07-28

    Carli Suspension Recalls Adjustable Track Bars for Ram Trucks

    Carli Suspension is recalling adjustable track bars for specific Ram trucks because a joint may break, causing loss of steering and increasing crash risk.

    Product
    SUSPENSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V482000·2017-07-28

    Chrysler Pacifica Recall: Rear Pinion Bracket Cracking Risk

    Vantage Mobility International is recalling 2017 Chrysler Pacifica lowered floor vehicles because rear pinion brackets may crack, causing wheel wobble and potential loss of control.

    Product
    CHRYSLER — CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V479000·2017-07-28

    Daimler Recalls 2010-2011 Sprinter Vehicles for Air Bag Inflator Rupture Risk

    Daimler Vans USA is recalling 2010-2011 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because passenger air bag inflators may rupture during deployment.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E041000·2017-07-28

    Dana Spicer Steer Axles Recalled for Potential Steering Loss

    Dana is recalling Spicer D-Series and E-Series steer axles because the castellated nut may not be properly torqued, allowing the tie rod to loosen and potentially disconnect.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V480000·2017-07-28

    Daimler Recalls 2012 Freightliner and Mercedes-Benz Sprinter Vehicles for Air Bag Defect

    Daimler Vans USA is recalling 2012 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because the passenger air bag inflators may rupture during deployment, posing a risk of serious injury or death.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17760·2017-07-28

    Nestlé Waters Recalls AccuPure Dispensers Due to Fire and Burn Hazards

    Nestlé Waters is recalling about 12,300 AccuPure floor-standing filtration dispensers because they can overheat, smoke, or catch fire. No injuries have been reported.

    Product
    AccuPure floor-standing filtration dispensers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V478000·2017-07-28

    Daimler Recalls 2007-2009 Sprinter Vehicles for Air Bag Inflator Defect

    Daimler Vans USA is recalling 2007-2009 Dodge and Freightliner Sprinter 2500 and 3500 vehicles because passenger air bag inflators may rupture in a crash.

    Product
    DODGE — DODGE, FREIGHTLINER SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V481000·2017-07-28

    BMW Recalls Motorcycles with Blocked Rear Reflex Reflectors

    BMW is recalling specific motorcycles because optional aluminum luggage cases may block rear reflex reflectors, increasing crash risk.

    Product
    BMW — BMW F800 GS, F650 GS, F800 GS ADVENTURE, F800 R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V476000·2017-07-27

    Nissan Recalls Infiniti Q50 and Q60 for Fuel Pump Software Defect

    Nissan is recalling 2016-2018 Infiniti Q50 and 2017 Q60 vehicles with 2.0L engines because faulty fuel pump software may cause the engine to stall while driving.

    Product
    INFINITI — INFINITI Q50, Q60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V477000·2017-07-27

    REV Recalls 2017-2018 Motorhomes With Non-Tempered Headlight Lenses

    REV Recreation Group is recalling 219 motorhomes because headlights may lack tempered glass lenses, which could crack and reduce visibility.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD, MONACO VACATIONER XE, ADMIRAL XE, STORM, FLAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2740-2017·2017-07-26

    Flowonix Recalls Prometra II Pump After Reported Fatal Overdose During MRI

    Flowonix Medical is recalling Prometra II implantable infusion pumps after a report of a fatal drug overdose during an MRI procedure.

    Product
    PROMETRA II Programmable Infusion Pump, Implantable Infusion Pump, Catalog Number/REF 13827, Part Number PL-31790-02. Manufactured by: Flowonix Medical Inc., --- The correction involves the labeling of the device plus the following Prometra II pump labeling is also being…
    Category
    Medical Device
    Distribution
    Distributed nationwide