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.

43426–43450 of 79632

  • HighFDA (Drugs)·D-0241-2018·2018-01-31

    DLC Laboratories Recalls Earth's Care Eczema Lotion Due to Microbial Contamination

    DLC Laboratories is recalling Earth's Care Eczema Lotion due to microbial contamination. The product was distributed nationwide.

    Product
    Earth's Care Eczema Lotion (2% Colloidal Oatmeal) Skin Protectant with Aloe and Almond Oil, 8 fl. oz. (237 mL) HPDE bottle, Distributed by: Earth's Care Natural Products, Inc. Long Beach, California 90805, NDC 24286-1569-08, UPC 85730700307.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0606-2018·2018-01-31

    Nestle HOT POCKETS Four Cheese Pizza Snack Bites Recalled for Missing Labeling

    Nestle USA is recalling 4,200 lbs of HOT POCKETS Four Cheese Pizza Snack Bites because the product was distributed without an ingredient statement or labeling, despite containing various allergens.

    Product
    Nestle HOT POCKETS¿ FOUR CHEESE PIZZA SNACK BITES in clear plastic bags.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0403-2018·2018-01-31

    Philips Brilliance iCT CT Systems Recalled for Software Defects

    Philips Medical Systems is recalling 559 Brilliance iCT CT systems due to software issues affecting scan functions and safety features.

    Product
    Brilliance iCT - Model 728306 Computed Tomography X-ray systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0236-2018·2018-01-31

    Ibuprofen Tablets Recalled Due to Odor Complaints and CGMP Deficiencies

    Marksans Pharma Inc. is recalling 4,127,500 ibuprofen tablets due to odor complaints and CGMP deficiencies. The product was distributed nationwide to repackaging firms.

    Product
    Ibuprofen Tablets, USP 200 mg, 6 x 6500 Tablets bulk packed in double polybag shipper packs for further packaging, Rx only, Manufactured by: Marksans Pharma Ltd., Plot No. L-82, L-83, Verna Indl. Estate, Verna, Goa - 403 722, India, NDC 25000-136-20.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0232-2018·2018-01-31

    Odan Laboratories Recalls Dry to Normal Skin Starter Kit for Stability Failure

    Odan Laboratories is recalling 179 kits of Dry to Normal Skin Starter Kit because the product failed stability specifications at 12 months.

    Product
    Dry to Normal Skin Starter Kit, Trousse debutante pour peau seche a normale. Kit includes: (Vegetable Cleanser (60 ml / 2 oz), Night Cream (15 g / 0.5 oz), Day Cream SPF15 {Octinoxate 7%, Avobenzone 2% and Oxybenzone 5%} (15 g / 0.5 oz), Eye Cream (6 g / 0.21 oz).Made in…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0238-2018·2018-01-31

    Marksans Pharma Recalls Ibuprofen Tablets Due to Odor Complaints

    Marksans Pharma Inc. is recalling 21,584,100 Ibuprofen Tablets, USP 400 mg, due to odor complaints linked to CGMP deficiencies.

    Product
    Ibuprofen Tablets, USP 400 mg, 6 x 3500 Tablets bulk packed in double polybag shipper packs for further packaging, Rx only, Manufactured by: Marksans Pharma Ltd., Plot No. L-82, L-83, Verna Indl. Estate, Verna, Goa - 403 722, India, NDC 25000-121-29.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0240-2018·2018-01-31

    Ibuprofen Tablets Recalled for Odor Complaints and CGMP Deficiencies

    Marksans Pharma Inc. is recalling 52,549,000 ibuprofen tablets due to odor complaints and CGMP deficiencies. The product was distributed nationwide.

    Product
    Ibuprofen Tablets, USP 800 mg, 6 x 1900 Tablets bulk packed in double polybag shipper packs for further packaging, Rx only, Manufactured by: Marksans Pharma Ltd., Plot No. L-82, L-83, Verna Indl. Estate, Verna, Goa - 403 722, India, NDC 25000-123-27.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0239-2018·2018-01-31

    Ibuprofen Tablets Recalled Due to Odor Complaints and CGMP Deficiencies

    Marksans Pharma Inc. is recalling specific lots of 600 mg ibuprofen tablets due to odor complaints linked to CGMP deficiencies.

    Product
    Ibuprofen Tablets, USP 600 mg, 6 x 2500 Tablets bulk packed in double polybag shipper packs for further packaging, Rx only, Manufactured by: Marksans Pharma Ltd., Plot No. L-82, L-83, Verna Indl. Estate, Verna, Goa - 403 722, India, NDC 25000-122-28.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0404-2018·2018-01-31

    Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler 45 Instruments

    Intuitive Surgical is recalling 60 da Vinci Xi EndoWrist Stapler 45 instruments due to a manufacturing variation that may prevent the release wrench from unclamping the device.

    Product
    daVinci X EndoWrist(R) Stapler 45, REF 470298 Product Usage: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads, and other Stapler Accessories (including the bladeless obturators) are intended to be used with the da Vinci Surgical System (Model IS4000) for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0231-2018·2018-01-31

    Odan Laboratories Recalls Day Cream SPF15 Due to Stability Failure

    Odan Laboratories is recalling 21 jars of Day Cream SPF15 because the product failed stability specifications at 12 months.

    Product
    Day Cream SPF15 Cr¿me de jour FPS 15, { Avobenzone 2%, Octinoxate 7%, Oxybenzone 5%} 15 ml / 0.5 fl. oz jar. Made in Canada, Kamins Dermatologics Inc. Montreal, Quebec H9R 2Y6. Distributed by Kamins Dermatologics Montreal, Quebec H9R 2Y6 Made in Fabrique au Canada. UPC code 6…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0235-2018·2018-01-31

    Ibuprofen Tablets Recalled for Odor Complaints and CGMP Deficiencies

    Marksans Pharma Inc. is recalling ibuprofen tablets due to odor complaints linked to Current Good Manufacturing Practice (CGMP) deficiencies.

    Product
    IBUPROFEN — IBUPROFEN (IBUPROFEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0395-2018·2018-01-31

    Measurement Specialties Reusable Temperature Probes Recalled for Unvalidated Sterilization Instructions

    Measurement Specialties Inc. is recalling 6,076 reusable temperature probes because their sterilization instructions have not been proven through a validation study.

    Product
    Measurement Specialties Reusable Temperature Probe Autoclavable. Sold as Esophageal/Rectal (Adult), Esophageal/Rectal (Pediatric), and Skin (Adult) Intended for use by a licensed physician to continuously monitor human esophageal, rectal, or skin temperature. They are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0230-2018·2018-01-31

    Mylan Recalls Bupropion HCL Extended-Release Tablets Due to Impurities

    Mylan Pharmaceuticals is voluntarily recalling specific bottles of bupropion HCL extended-release tablets due to out-of-specification impurities found during routine stability testing.

    Product
    bupPROPion HCL Extended-Release Tablets, USP (XL) 300 mg, 500-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. NDC: 0378-2009-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V080000·2018-01-30

    Forest River Recalls 2018 Georgetown RVs Due to Wiring Fire Risk

    Forest River is recalling 2018 Georgetown recreational vehicles because undersized wiring may melt and cause a fire. Dealers will install an additional circuit breaker free of charge.

    Product
    FOREST RIVER — FOREST RIVER GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V082000·2018-01-30

    Audi Recalls Vehicles Due to Driver Air Bag Inflator Explosion Risk

    Volkswagen Group of America is recalling specific Audi models because the driver's air bag inflator may explode during deployment, potentially causing serious injury or death.

    Product
    AUDI — AUDI S5 CABRIOLET, S4 CABRIOLET, A3, A4 CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V077000·2018-01-30

    Entegra Recalls Aspire and Insignia Motorhomes Due to Brake Reservoir Defect

    Entegra is recalling 2015-2018 Aspire and Insignia motorhomes because the air brake supply reservoir is undersized, which may reduce braking performance and increase crash risk.

    Product
    ENTEGRA — ENTEGRA INSIGNIA, ASPIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E007000·2018-01-30

    Lippert Components Recalls Ford F53 Chassis for Driveshaft Misalignment

    Lippert Components is recalling specific Ford F53 chassis used in Coachmen and Mirada RVs because a misaligned driveshaft may cause excessive vibration and potential vehicle disablement.

    Product
    STRUCTURE:FRAME AND MEMBERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V083000·2018-01-30

    Thomas Built Buses Recall Fire Extinguishers Due to Clogging and Injury Risk

    Daimler Trucks North America is recalling 2002-2017 Thomas Built Buses equipped with specific Kidde fire extinguishers that may clog or detach, posing injury risks.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, FS-65, SAF-T-LINER C2, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V079000·2018-01-30

    Eclipse Recalls 2019 Attitude Trailers Due to Incorrect Tire Load Range

    Eclipse Recreational Vehicles is recalling 2019 Attitude trailers equipped with tires that have the incorrect load range, which may lead to tire failure and increase crash risk.

    Product
    ECLIPSE — ECLIPSE ATTITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18086·2018-01-30

    Walgreens Pain and Itch Relief Cream Recalled for Packaging Safety

    Natureplex is recalling Well at Walgreens pain and itch relief cream because the packaging is not child-resistant, posing a poisoning risk to young children.

    Product
    Well at Walgreens pain and itch relief cream
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V078000·2018-01-30

    Jayco Recalls 2017 Precept Motorhomes Due to Brake Fluid Leak Risk

    Jayco is recalling 2017 Precept motorhomes because missing valve block ball plugs in the brake system may cause fluid leaks or air ingestion, increasing stopping distance.

    Product
    JAYCO — JAYCO PRECEPT
    Category
    Vehicle
    Distribution
    Distributed nationwide