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.

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.

49901–49925 of 79640

  • HighNHTSA·16V767000·2016-10-21

    KME Predator Aerial Vehicles Recalled for Water Way Trolley Separation Risk

    KME is recalling certain Predator aerial emergency vehicles because the water way trolley could separate from the ladder, posing a falling object hazard.

    Product
    KME — KME PREDATOR SS AERIAL, PREDATOR AERIAL, PREDATOR PANTHER AERIAL, PREDATOR TDA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17704·2016-10-20

    Summer Classics Recalls Swivel Rocking Lounge Chairs Due to Fall Hazard

    Summer Classics is recalling about 800 swivel rocking lounge chairs because the seat bucket can break away from the base, posing a fall hazard. No injuries have been reported.

    Product
    Swivel rocking lounge chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V761000·2016-10-20

    Entegra Recalls 2016-2017 Motorhomes Due to Flammable Mattress

    Entegra is recalling 2016-2017 Cornerstone and Anthem motorhomes because the Tempurpedic Sealy Mattress may burn quickly, violating federal flammability standards.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V760000·2016-10-20

    Mercedes-Benz Recalls S-Class Vehicles for Headlight Adjustment Defect

    Mercedes-Benz is recalling 996 S-Class vehicles because improperly adjusted low-beam headlights may reduce driver visibility and increase crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG S63, S65 AMG, AMG S65, S550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17018·2016-10-20

    Cabela's Recalls Commercial Food Dehydrators Due to Fire Hazard

    Cabela's is recalling commercial food dehydrators because defective wiring can cause heat build-up and fire. No injuries have been reported.

    Product
    Cabela's food dehydrators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V762000·2016-10-20

    Forest River Cedar Creek Recalled for Incorrect Axle Capacity Ratings

    Forest River is recalling 2017 Cedar Creek trailers because axles were misidentified as having a 7,000-pound capacity when they are only rated for 6,000 pounds.

    Product
    FOREST RIVER — FOREST RIVER CEDAR CREEK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17019·2016-10-20

    Makita Recalls 5057KB Circular Saws Due to Laceration Hazard

    Makita is recalling about 450 5057KB circular saws because the lower blade guard can malfunction and expose the blade, posing a laceration risk.

    Product
    Circular saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0006-2017·2016-10-19

    Uncle Buck's Maple Nut Candy Recalled for Undeclared Peanut Allergen

    Rucker's Wholesale & Service Co. is recalling Uncle Buck's Maple Nut candy because the label fails to list peanuts, a major allergen, as an ingredient.

    Product
    Uncle Buck's Maple Nut candy packaged in a clear plastic 2.7 oz. bag with attached green, orange, and white label with Organe and black writing.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0087-2017·2016-10-19

    NatureBox Dark Cocoa Nom Noms Recalled for Undeclared Peanut Allergen

    NatureBox is recalling Dark Cocoa Nom Noms because some bags may contain peanut butter but do not list peanuts on the label.

    Product
    Dark Cocoa Nom Noms 4.5oz. (128g) UPC: 8 54557 00533 5 Lot 16083 Product is shipped directly to customers per individual order or to corporate customers in 20 x 4.5 oz. bags cases. Ingredients: Rolled Oats, Almonds. For address freshness (Grape juice, rice dextrin)…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0094-2017·2016-10-19

    B. Braun Recalls 5% Dextrose Injection Due to Fungal Contamination

    B. Braun Medical Inc. is recalling 57,408 units of 5% Dextrose Injection USP due to non-sterility caused by fungal contamination from leaking containers.

    Product
    5% Dextrose Injection USP, 100mL in a 150 mL PAB container, Rx only, B. Braun Medical Inc. Irvine, CA 92614-5895 USA, NDC 00264-1510-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0047-2017·2016-10-19

    Quaker Quinoa Granola Bars Recalled Due to Listeria Risk

    The Quaker Oats Company is recalling Quaker Quinoa Granola Bars because sunflower kernels used in their production were linked to a Listeria monocytogenes recall.

    Product
    Quaker Quinoa Granola Bars, chocolate nut medley packaged in a multi colored box with brown lettering. Wrapper UPC: 000 30000 00243 8
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0022-2017·2016-10-19

    Diocto Liquid Stool Softener Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Diocto Liquid stool softener bottles due to positive findings of Burkholderia cepacia contamination.

    Product
    Diocto Liquid (docusate sodium) 50 mg/5 mL Stool Softener Laxative, One Pint (473 mL) bottles, Dist by: Rugby Laboratories, Livonia, MI --- NDC 0536-0590-85
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0048-2017·2016-10-19

    Quaker Quinoa Granola Bars Recalled Due to Listeria Risk

    The Quaker Oats Company is recalling Quaker quinoa granola bars because they were made with sunflower kernels contaminated with Listeria monocytogenes.

    Product
    Quaker quinoa granola bars, yogurt fruit and nut flavor packaged in a multi colored box with brown lettering. Wrapper UPC: 000 30000 00195 0
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0049-2017·2016-10-19

    Pharmedium Recalls Heparin Sodium Syringes Due to Subpotency and Stability Concerns

    Pharmedium Services, LLC is recalling 350 syringes of Heparin Sodium Injection USP because confirmed subpotency and stability data do not support the expiry date.

    Product
    HEPARIN Sodium Inj. USP, 3,000 USP Heparin Units per 3 mL Total Volume in a syringe, NOT FOR LOCK FLUSH, 1,000 Heparin USP Units per mL, Rx only, PharMEDium, Product code 2K1926.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0016-2017·2016-10-19

    Leiter's Compounding Recalls Moxifloxacin Intravitreal Injection Due to Sterility Concerns

    Leiter's Compounding is recalling Moxifloxacin intravitreal injections because they were produced using recalled filters, raising concerns about sterility.

    Product
    Moxifloxacin 1 mg/mL in Sterile Balanced Salt Solution (BSS) Intravitreal Injection, 1 mL Total Volume in a 2 mL Vial, Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-003-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0007-2017·2016-10-19

    Cabela's Maple Nut Candies Recalled for Undeclared Peanut Allergen

    Rucker's Wholesale & Service Co. is recalling Cabela's Maple Nut candies because the label fails to list peanuts, a major allergen.

    Product
    Cabela's classic candies Maple nut packaged in 2.7 oz. clear plast ice bag with brown label attached with brown lettering.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0049-2017·2016-10-19

    Nature's Power Solutions Acidophilus Blend Recalled for Undeclared Milk

    Complete Packaging & Manufacturing is recalling Nature's Power Solutions Acidophilus Blend dietary supplements because they contain undeclared milk, a major food allergen.

    Product
    Dietary Supplement Acidophilus Blend, 90 capsules, Product No. E-420, packaged in 225cc HDPE white bottle, room temp, sold individually
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0055-2017·2016-10-19

    Publix Maple Walnut Strip Danish Recalled for Metal Shavings

    Gold Standard Baking is recalling Publix Maple Walnut Strip Danishes due to the presence of small metal shavings.

    Product
    Publix Maple Walnut Strip Danish | Count, 1 | NET WT 14.00 oz | Distributed by Publix Supermarkets, Inc., Lakeland, FL 33802
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0034-2017·2016-10-19

    Pharmedium Recalls Fentanyl Citrate Injection Due to Subpotency and Stability Issues

    Pharmedium Services, LLC is recalling specific lots of fentanyl citrate injection because confirmed subpotency and stability data do not support the expiry date.

    Product
    fentaNYL Citrate Injection, 50 mcg per mL, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3153.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0096-2017·2016-10-19

    Hospira Recalls Marcaine Injection Due to Sterility and Potency Issues

    Hospira is recalling 15 vials of Marcaine 0.25% injection because a glass defect allowed water to enter, compromising sterility and reducing drug potency.

    Product
    MARCAINE — MARCAINE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0011-2017·2016-10-19

    Leiter's Compounding Recalls Brilliant Blue G Injection Due to Sterility Concerns

    Leiter's Compounding is recalling Brilliant Blue G injections because they were produced using recalled filters, raising concerns about sterility.

    Product
    Brilliant Blue G 0.025% in 0.9% Sodium Chloride (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-008-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0067-2017·2016-10-19

    Publix Cherry Strip Danish Recalled for Metal Shavings

    Gold Standard Baking is recalling Publix Cherry Strip Danishes due to the presence of small metal shavings.

    Product
    Publix Cherry Strip Danish | Count, 1 | NET WT 15.00 oz | Distributed by Publix Supermarkets, Inc., Lakeland, FL 33802. UPC: 002-19562-00000
    Category
    Food
    Distribution
    Distributed nationwide