The Recall Desk

State

Oklahoma product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55076–55100 of 79650

  • SevereNHTSA·15V820000·2015-12-07

    Polaris Recalls 2015 GEM Electric Vehicles for Seat Belt Defect

    Polaris is recalling 2015 GEM electric vehicles because seat belt retractors may fail, preventing proper occupant restraint in a crash.

    Product
    GEM — GEM E6S, E4, ELXD, EL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V816000·2015-12-07

    Freightliner Cascadia CNG Vehicles Recalled for Exhaust Fire Risk

    Daimler Trucks North America is recalling 2013-2015 Freightliner Cascadia CNG vehicles because hot exhaust near the pressure relief device may cause gas release and fire.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V821000·2015-12-07

    Honda Recalls VFR1200F Motorcycles for Driveshaft Universal Joint Wear

    Honda is recalling 2010, 2012, and 2013 VFR1200F motorcycles because driveshaft universal joint bearings may wear prematurely, potentially causing the joint to separate or break.

    Product
    HONDA — HONDA VFR1200F
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V819000·2015-12-07

    Tiny Idahomes Recalls RVs With Overheating Water Heater Valves

    Tiny Idahomes is recalling 2014-2016 RVs equipped with specific Atwood water heaters that may overheat water, posing a scalding risk.

    Product
    TINY IDAHOMES — TINY IDAHOMES CASCADE, CLEAR CREEK, CARPATHIAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V814000·2015-12-03

    ShowHauler Recalls One 2013 Motorhome Due to Water Heater Overheating

    ShowHauler Trucks is recalling one 2013 ShowHauler motorhome because a defective water heater valve may cause water to overheat, posing a scalding risk.

    Product
    SHOWHAULER — SHOWHAULER MOTORHOME
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0224-2016·2015-12-02

    Frozen Cookie Dough Recalled for Undeclared Milk, Soy, and Wheat

    Tower Cafe Inc. is recalling 1,424 tubs of Chocolate Chip Old Fashioned Gourmet Cookie Dough sold in Oklahoma due to undeclared milk, soy, and wheat allergens.

    Product
    Chocolate Chip Old Fashioned Gourmet Cookie Dough NET WT. 3 lb. (48 oz.) Distributed By: Tower Cafe, Okarche, OK 73762 packaged in plastic tub.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0265-2016·2015-12-02

    TN Juice Bar Recalls Refine 3-Day Cleanse Juice Kit Nationwide

    TN Juice Bar is recalling 137 units of the Refine 3-Day Cleanse juice kit nationwide due to unpasteurized juice with elevated pH levels and unlabeled almond milk.

    Product
    Refine 3-Day Cleanse, a juice kit that contains Lean Green, 16 oz (6 bottles), Beet It, 16 oz (6 bottles), Almond Milk, 8 oz (3 bottles) and Wheat grass juice, 8 oz (2 bottles)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V812000·2015-12-02

    Ford Recalls 2013 Vehicles for Fuel Delivery Module Fire Risk

    Ford is recalling 2013 Explorer, Taurus, Flex, Lincoln MKS, and MKT vehicles because a cracked fuel delivery module may leak fuel and cause a fire.

    Product
    FORD — FORD, LINCOLN TAURUS, MKT, FLEX, MKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0223-2016·2015-12-02

    Tower Cafe Frozen Cookie Dough Recalled for Undeclared Allergens

    Tower Cafe is recalling 656 tubs of M&M Old Fashioned Gourmet Cookie Dough sold in Oklahoma due to undeclared milk, soy, wheat, and yellow #5.

    Product
    M&M Old Fashioned Gourmet Cookie Dough NET WT. 3 lb. (48 oz.) Distributed By: Tower Cafe, Okarche, OK 73762 packaged in plastic tub.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0327-2016·2015-12-02

    NxStage System One S Cycler Recalled for Ultrafiltration Software Error

    NxStage Medical is recalling 16 System One S Cycler units due to a software error causing inaccurate fluid removal.

    Product
    NxStage System One S Cycler (High Permeability Hemodialysis System) Model no. NX1000-5-A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0331-2016·2015-12-02

    Palindrome Precision Chronic Catheter Kit Recalled for Packaging Defect

    Covidien LLC is recalling 365 units of Palindrome Precision Chronic Catheter Kits because they were incorrectly packaged with a 90-degree bend at the distal tip.

    Product
    Palindrome Precision Chronic Catheter Kit Symmetrical Tip, Tal VenaTrac" Stylet 14.5 Fr/Ch (4.8mm) X 33 cm Item Number: 8888145042P The Palindrome chronic catheter is intended for acute and chronic hemodialysis, apheresis, and infusion. It may be inserted either…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0225-2016·2015-12-02

    Frozen Cookie Dough Recalled for Undeclared Soy and Wheat

    Tower Cafe Inc. is recalling 480 tubs of Sugar Old Fashioned Gourmet Cookie Dough in Oklahoma due to undeclared soy and wheat allergens.

    Product
    Sugar Old Fashioned Gourmet Cookie Dough NET WT. 3 lb. (48 oz.) Distributed By: Tower Cafe, Okarche, OK 73762 packaged in plastic tub.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0386-2016·2015-12-02

    Qualgen Recalls Estradiol Pellets Due to Sterility Assurance Concerns

    Qualgen is recalling 4,221 vials of compounded Estradiol USP pellets nationwide because deficient practices may have impacted sterility assurance.

    Product
    Estradiol USP 99.5%, .5% Stearic Acid NF Pellets, 3 mL, one-count vials, 6 mg (NDC 69761-006-01),10 mg (NDC 69761-010-01),12.5 mg (NDC 69761-012-01), 15 mg (NDC 69761-015-01),18 mg (NDC 69761-018-01),20 mg (NDC 69761-020-01), 22 mg (NDC 69761-022-01), 25 mg (NDC 69761-025-01)…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0320-2016·2015-12-02

    Philips HeartStart MRx Monitor/Defibrillator Recalled for Software Issue

    Philips is recalling HeartStart MRx Monitor/Defibrillators because a software issue may cause the automated Ready-For-Use test to stop in an abnormal state when the device is turned off.

    Product
    Philips HeartStart MRx Monitor/Defibrillator; M3535A, M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6. For use for the termination of ventricular tachycardia and ventricular fibrillation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0226-2016·2015-12-02

    Tower Cafe Oatmeal Raisin Cookie Dough Recalled for Undeclared Soy and Wheat

    Tower Cafe Inc. is recalling 596 tubs of Oatmeal Raisin Old Fashioned Gourmet Cookie Dough sold in Oklahoma due to undeclared soy and wheat allergens.

    Product
    Oatmeal Raisin Old Fashioned Gourmet Cookie Dough NET WT. 3 lb. (48 oz.) Distributed By: Tower Cafe, Okarche, OK 73762 packaged in plastic tub.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0326-2016·2015-12-02

    NxStage System One S Cycler Recalled for Ultrafiltration Software Error

    NxStage Medical is recalling 323 System One S Cycler units due to a software error that may cause inaccurate fluid removal during hemodialysis.

    Product
    NxStage System One S Cycler (High Permeability Hemodialysis System) Model no. NX1000-5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0387-2016·2015-12-02

    Qualgen Recalls Testosterone Pellets Due to Sterility Assurance Concerns

    Qualgen is recalling 10,885 vials of compounded Testosterone USP pellets nationwide due to deficient practices that may impact sterility assurance.

    Product
    Testosterone USP 99.5%, .5% Stearic Acid NF Pellets, 3 mL, one-count vials, 25 mg (NDC 69761-125-01), 37.5 mg (NDC 69761-137-01), 50 mg (NDC 69761-150-01), 87.5 mg (NDC: 69761-187-01), 100 mg (NDC 69761-110-01), 200 mg (NDC 69761-120-01), Rx only, Compounded by Qualgen, Edmond…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0333-2016·2015-12-02

    Palindrome Precision Chronic Catheter Kit Recalled for Packaging Defect

    Covidien LLC is recalling 10 units of Palindrome Precision Chronic Catheter Kits due to incorrect packaging with a 90-degree bend at the distal tip.

    Product
    Palindrome Precision Chronic Catheter Kit Symmetrical Tip, Pre-Curved Shaft and Tal VenaTrac" Stylet 14.5 Fr/Ch (4.8mm) X 33 cm Item Number: 8888145061P The Palindrome chronic catheter is intended for acute and chronic hemodialysis, apheresis, and infusion. It may be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0323-2016·2015-12-02

    CSM Bakery Recalls Daily Chef Peanut Butter Bars Due to Foreign Matter

    CSM Bakery Products NA is recalling Daily Chef Peanut Butter Bars because rigid plastic pieces were found in the product.

    Product
    Daily Chef Peanut Butter Bars, Net Wt. 27 oz (1 lb 11 oz) 765g, Made in Canada, Manufactured for: CSM Bakery Products NA, Inc., Tucker, GA 30084
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-0338-2016·2015-12-02

    Masimo Recalls Rainbow Reusable Sensors Due to Inaccurate Readings

    Masimo is recalling Rainbow Reusable Sensors because incompatible configurations may cause no readings or inaccurate SpCO and SpMet results.

    Product
    rainbow Reusable Sensors. RAINBOW DCI-DC3, SpO2/SpCO/SpMet, Part No. 2201; RAINBOW DCI-dc8, SpO2/SpCO/SpMet, Part No. 2407; RAINBOW DCI, SpO2/SpCO/SpMet, Part No. 2696; RAINBOW DCIP, PED, SpO2/SpCO/SpMet, Part No. 2697. rainbow reusable sensors are indicated for spot check…
    Category
    Medical Device
    Distribution
    Distributed nationwide