The Recall Desk

State

Oklahoma product recalls

73,833 recalls have nationwide distribution and so reach Oklahoma. 5,824 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,824
Critical
1,040
Severe
1,494
Most recent
2026-11-14

Of the 5,824 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 5,824 recalls whose distribution notice names Oklahoma specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59526–59550 of 79657

  • HighCPSC·15109·2015-04-14

    San Pedro Manufacturing Recalls Renovated Mattresses and Foundations

    San Pedro Manufacturing is recalling about 4,800 renovated mattresses and foundations because they fail to meet federal fire safety standards.

    Product
    Mattresses and Mattresses with Foundations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·060-2015·2015-04-13

    Leader Slaughterhouse Recalls Veal Carcasses Produced Without Full Federal Inspection

    Leader Slaughterhouse, LLC is recalling approximately 1,800 pounds of veal carcasses produced without the full benefit of federal inspection. The product was distributed to customers in Pennsylvania and New York.

    Product
    Leader Slaughterhouse, LLC — Leader Slaughterhouse, LLC Recalls Veal Carcasses Produced Without Full Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V215000·2015-04-13

    Crossroads Recalls 2016 Recreational Trailers Due to Wheel Stud Defect

    Crossroads is recalling 2016 recreational trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.

    Product
    CROSSROADS — CROSSROADS ELEVATION, HAMPTON, REZERVE, SUNSET TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V214000·2015-04-10

    Land Rover Recalls 2015 LR4 Models Due to ABS Software Error

    Land Rover is recalling 2015 LR4 vehicles because an ABS software error may disable stability and traction control systems, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER LR4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V211000·2015-04-10

    Spartan Recalls 2015 K3 Chassis Due to Tag Axle Suspension Defect

    Spartan Motors is recalling 66 model year 2015 K3 chassis because tag axle suspension hangers may move, causing the axle to shift off center and increasing crash risk.

    Product
    SPARTAN — SPARTAN K3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1869-2015·2015-04-08

    Horizon Cheddar Sandwich Crackers Recalled for Undeclared Peanuts

    WhiteWave Foods is recalling Horizon Cheddar Sandwich Crackers because they may contain undeclared peanuts due to a packaging error.

    Product
    Organic Horizon Sandwich Crackers Cheddar, 7.5 oz packages, 12 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1791-2015·2015-04-08

    HT Traders Blue Cheese Jalapeno Seasoning Blend Recalled for Undeclared Peanut

    Brinkhoff & Monoson Inc is recalling HT Traders Blue Cheese Jalapeno Spicy & Unique Seasoning Blend because it may contain undeclared peanut allergens.

    Product
    HT Traders Blue Cheese Jalapeno Spicy & Unique Seasoning Blend packaged in a 6 oz clear square glass bottle with a black metal cap and a label weight of 3.7 oz (104.9 g), Proudly Distributed by Harris Teeter, LLC., Matthews, NC;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0428-2015·2015-04-08

    Baxter Recalls Clinimix E Due to Sterility Assurance Concerns

    Baxter Healthcare is recalling 7,444 containers of Clinimix E 5/20 due to a lack of assurance of sterility and increased leak complaints.

    Product
    CLINIMIX E — CLINIMIX E (LEUCINE, PHENYLALANINE, LYSINE, METHIONINE, ISOLEUCINE, VALINE, HISTIDINE, THREONINE, TRYPTOPHAN, ALANINE, GLYCINE, ARGININE, PROLINE, SERINE, TYROSINE, DIBASIC POTASSIUM PHOSPHATE, MAGNESIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1362-2015·2015-04-08

    Pega Medical Recalls GAP Nail 4.8mm Due to Distal Screw Hole Failures

    Pega Medical Inc. is recalling 7 units of the 4.8mm GAP Nail because of failures at the distal cortical screw holes, primarily in patients with specific bone conditions.

    Product
    GAP Nail 4.8mm (diameter size) of the GAP ENDO-EXO MEDULLARY SYSTEM. Catalog number GAP-N48-16; GAP-N48-18; GAP-N48-26; GAP-N48-28. Product Usage: The GAP Endo-Exo Medullary System is used for the treatment of fractures or correction of deformities in the femur, tibia and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1356-2015·2015-04-08

    Medtronic Temporary Pacemaker Recalled for Battery Connection Failure

    Medtronic is recalling 6,040 Model 5392 temporary pacemakers because specific AA batteries may fail to connect, potentially stopping pacing therapy.

    Product
    Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a cardiac pacing lead system for temporary single or dual chamber pacing in a clinical environment by trained personnel. The temporary pacemaker can be used…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1874-2015·2015-04-08

    Healthy Mama Protein Drink Recalled for Undeclared Milk Allergen

    Maternal Science Inc. is recalling Healthy Mama Boost It Up Mighty Mango Protein Drink because it contains undeclared milk.

    Product
    Healthy Mama Boost It Up Mighty Mango Caffeine Free Protein with Energy Drink 12 fl oz Distributed by: Maternal Science, Inc. 50 Tice Boulevard, Suite 340 Woodcliff Lake, NJ 07677 UPC 810758020058
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1803-2015·2015-04-08

    My Spice Sage Ground Cumin Recalled for Undeclared Peanut

    Zenobia Company LLC is recalling My Spice Sage Ground Cumin because it may contain undeclared peanut protein. The recall covers 1,467 units sold nationwide.

    Product
    My Spice Sage CUMIN GROUND under the following labels and packaging: 1) NET WT 1 oz (28g) UPC 00105001, packed in a plastic resealable bag 2) NET WT 4 oz (113g) UPC 00105004 packed in a plastic resealable bag, 3) NET WT 4.9 oz (139g) UPC 00105000 packed in a plastic bottle, 4)…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1872-2015·2015-04-08

    Healthy Mama Boost It Up Protein Drink Recalled for Undeclared Milk

    Maternal Science Inc. is recalling Healthy Mama Boost It Up Mango with Ginger Protein Drink because it contains undeclared milk.

    Product
    Healthy Mama Boost it Up Mango with Ginger Caffeine Free Protein with Energy Drink 12 fl oz Distributed by: Maternal Science, Inc. 50 Tice Boulevard, Suite 340 Woodcliff Lake, NJ 07677 UPC 810758020058
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V210000·2015-04-08

    KTM Recalls 2015 690 Enduro R Motorcycles Due to Rear Brake Line Damage

    KTM is recalling 409 model year 2015 690 Enduro R motorcycles because the rear brake line may be damaged, potentially causing a loss of braking ability and increasing crash risk.

    Product
    KTM — KTM 690 ENDURO R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1370-2015·2015-04-08

    BD FACSCalibur Instruments Recalled for Incorrect Circuit Breaker Amperage

    BD Biosciences is recalling 72 BD FACSCalibur instruments because some have circuit breakers with incorrect amperage ratings, which may fail to open during over-current situations.

    Product
    BD FACSCalibur; Catalog Numbers 342973, 342975, 34976 In vitro Diagnostics Use.
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Food)·F-1790-2015·2015-04-08

    Archer Farms Ground Cumin Recalled for Undeclared Peanut Allergen

    Brinkhoff & Monoson Inc is recalling Archer Farms ground cumin because it may contain undeclared peanut allergens.

    Product
    Archer Farms Cumin, ground, packaged in 6 oz clear square glass bottle with a silver metal cap and a label weight of 2.8oz (79 g), Distributed by Target Corp. Minneapolis, MN;
    Category
    Food
    Distribution
    Distributed nationwide