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.

Which agencies issued them

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.

50751–50775 of 79640

  • SevereFDA (Food)·F-2034-2016·2016-09-07

    Hampton Creek White Cake Mix Recalled for Salmonella Risk

    Hampton Creek Foods is recalling JUST White Cake Mix because a positive test for Salmonella was found in the coconut milk powder used in its manufacturing.

    Product
    JUST White Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567 g); UPC 8 54829 00688 6. Ingredients: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour, niacin, reduced Iron…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2007-2016·2016-09-07

    Raw Pistachio Kernels Recalled Due to Salmonella Contamination

    International Foodsource LLC is recalling 9,756 bags of Valued Natural Raw Pistachio Kernels due to potential Salmonella contamination.

    Product
    Valued Natural Raw Pistachio Kernels Net Wt 5 oz. (141 g) International Foodsource LLC 52 Richboynton, Rd. Dover, NJ 07801 UPC 790429241428
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2036-2016·2016-09-07

    Warren Produce Recalls Serrano Peppers Due to Salmonella Contamination

    Warren Produce is recalling 14,000 pounds of Primo Fresh Serrano Peppers because the product tested positive for Salmonella.

    Product
    Primo Fresh Serrano Peppers Distributed by Warren Produce, 824 W. Monte Cristo Rd, Edinburg, TX packaged in 1/4 bushel waxed cardboard boxes, 1 1/9 bushel waxed cardboard boxes, 10 lb waxed cardboard boxes, 5 lb waxed cardboard boxes and 35 lb RPC crates.
    Category
    Food
    Distribution
    10 states
  • SevereNHTSA·16V646000·2016-09-07

    Audi Recalls 2012-2013 A6 and A7 for Fuel Hose Leak Risk

    Volkswagen Group of America is recalling 28,249 Audi A6 and A7 vehicles because a fuel hose may degrade and leak, increasing fire risk.

    Product
    AUDI — AUDI A7, A6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2013-2016·2016-09-07

    Big Pig Bacon Seasoning Salt Recalled for E. coli O121 Contamination Risk

    J&D's Down Home Enterprises is recalling Big Pig Original Bacon Flavored Seasoning Salt due to potential E. coli O121 contamination.

    Product
    Original Bacon Flavored Seasoning Salt, Big Pig brand, 16oz plastic jars, 3 jars per case. UPC 98300 00110
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2676-2016·2016-09-07

    Intuitive Surgical Recalls da Vinci EndoWrist Stapler 30 Instruments

    Intuitive Surgical is recalling 875 da Vinci EndoWrist Stapler 30 instruments due to reported field failures involving shaft rotation interruption or jaws not opening.

    Product
    STAPLER 30,IS4000; Model number 470430; General and Plastic Surgery: The Intuitive Surgical da Vinci EndoWrist Stapler 30 Instrument and Stapler 30 Reloads are intended to be used with the da Vinci Xi Surgical System (Model IS4000) for resection, transection and/or creation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2677-2016·2016-09-07

    Intuitive Surgical Recalls da Vinci EndoWrist Stapler 30 Instruments

    Intuitive Surgical is recalling 875 da Vinci EndoWrist Stapler 30 instruments due to reported shaft rotation interruptions and jaw opening failures.

    Product
    CURVED-TIP STAPLER 30,IS4000; Model number 470530; General and Plastic Surgery: The Intuitive Surgical da Vinci EndoWrist Stapler 30 Instrument and Stapler 30 Reloads are intended to be used with the da Vinci Xi Surgical System (Model IS4000) for resection, transection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V647000·2016-09-07

    Volkswagen and Audi Recall 2015-2016 Models for Fuel Leak Fire Risk

    Volkswagen is recalling 2015-2016 Golf, GTI, and Audi A3 vehicles because a faulty fuel pump may cause leaks that increase fire risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI GOLF, GTI, A3 CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2016-2016·2016-09-07

    Hampton Creek Muffin Mix Recalled for Salmonella in Coconut Milk Powder

    Hampton Creek Foods is recalling JUST Chocolate Chunk Muffin Mix because a positive test result for Salmonella was found in the coconut milk powder used in manufacturing.

    Product
    JUST Chocolate Chunk Muffin Mix; NET WT 20.8 oz. (1 lb 4.8 oz) 590 g); UPC 8 54829 00656 5. Ingredients: Muffin Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2018-2016·2016-09-07

    Hampton Creek Blueberry Muffin Mix Recalled for Salmonella Risk

    Hampton Creek Foods is recalling JUST Blueberry Muffin Mix because a positive test for Salmonella was found in the coconut milk powder used to make it.

    Product
    JUST Blueberry Muffin Mix; NET WT 23.3 oz. (1 lb 7.3 oz) 660 g); UPC 8 54829 00685 5. Ingredients: Muffin Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2035-2016·2016-09-07

    Hampton Creek Cinnamon Roll Coffee Cake Mix Recalled for Salmonella

    Hampton Creek Foods is recalling JUST Cinnamon Roll Coffee Cake Mix because a positive test for Salmonella was found in the coconut milk powder used in its manufacturing.

    Product
    JUST Cinnamon Roll Coffee Cake Mix; NET WT 26.9 oz. (1 lb 10.9 oz) 762 g); UPC 8 54829 00644 2. Ingredients: Cake Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2019-2016·2016-09-07

    Hampton Creek Devil's Food Cake Mix Recalled for Salmonella

    Hampton Creek Foods is recalling Devil's Food Cake Mix because a positive test found Salmonella in the coconut milk powder used in manufacturing.

    Product
    JUST Devil's Food Cake Mix; NET WT 20 oz. (1 lb 4 oz) 567 g); UPC 8 54829 00643 5. Ingredients: Muffin Mix: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour, niacin…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2017-2016·2016-09-07

    Hampton Creek Recalls JUST Yellow Cake Mix Due to Salmonella Risk

    Hampton Creek Foods is recalling JUST Yellow Cake Mix because a positive test for Salmonella was found in the coconut milk powder used to make it.

    Product
    JUST Yellow Cake Mix; NET WT 20 z. (1 lb 4oz) 567 g); UPC 8 54829 00642 8. Ingredients: Enriched flours, {bleached (wheat flour, niacin, reduced Iron, thiamine mononitrate, riboflavin, folic acid), unbleached (Wheat flour, malted barley flour, niacin, reduced Iron…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2692-2016·2016-09-07

    Beckman Coulter Recalls UniCel DxH Slidemaker Stainer Due to Fire Risk

    Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer because flammable liquids may contact electrical components, posing a fire hazard.

    Product
    UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Catalog No. 775222 UniCel DxH Slidemaker Stainer (DxH SMS) Instructions for Use (IFU) Part Number B26647AC The DxH Slidemaker Stainer is a fully automated slide preparation and staining device that aspirates a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2008-2016·2016-09-07

    IFS Raw Shelled Pistachios Recalled for Potential Salmonella Contamination

    International Foodsource LLC is recalling raw shelled pistachios due to potential Salmonella contamination found in FDA testing.

    Product
    IFS Club Bag Pistachio Raw Shelled 80% Wholes Net Wt. 3 lb. (1 kg) International Foodsource LLC 52 Richboynton Rd. Dover NJ 07801 UPC 790429243026
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2673-2016·2016-09-07

    Nakanishi Diamond Coated Tips Recalled for Missing Single-Use Labeling

    Nakanishi Inc. is recalling 2,574 diamond coated tips and burs because the labeling failed to indicate they are single-use only, posing a cross-contamination risk.

    Product
    Diamond Coated Tips and Burs are accessories to the air powered Bone drill (VARIOSURG with and without light) The intended use of the tips is based on the parent device. For the VarioSurg, in addition to the scaling functions, diamond coated tips are used for socket lift, sinus…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2713-2016·2016-09-07

    Cardinal Health Recalls Arterial Blood Gas Kits Missing Safety Clasp

    Cardinal Health is recalling specific lots of 9025TRU Arterial Blood Gas Kits because they are missing a locking clasp component, posing a potential safety risk.

    Product
    The 9025TRU Arterial Blood Gas (ABG) Kit is used to obtain arterial blood sampling for pH, Blood Gas, Electrolyte and Metabolite Analysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2709-2016·2016-09-07

    Merge Cardio software recall due to incorrect patient data saving

    Merge Healthcare is recalling Merge Cardio software versions 10.1 and 10.1.1 because reports may be saved to incorrect patient records.

    Product
    Merge Cardio software. The firm name on the label is Merge Healthcare, Hartland, WI. Image processing system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V645000·2016-09-07

    Forest River Recalls 2017 Coachmen Viking Trailers Due to Roof Strut Defect

    Forest River is recalling 2017 Coachmen Viking recreational trailers because a missing wire clip may allow the roof strut to detach, causing the roof to drop and increasing injury risk.

    Product
    COACHMEN — COACHMEN VIKING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2691-2016·2016-09-07

    Elekta Recalls HexaPOD evo RT Systems for Positioning Errors

    Elekta is recalling 13 HexaPOD evo RT Systems because the treatment couch may not move fully to the correct 3D position, potentially leading to unrecognized positioning errors during radiotherapy.

    Product
    HexaPOD evo RT System Product Usage: The intended use of the device is the control of accurate patient positioning with assistance of a 3D Tracking System in a radiotherapy environment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1992-2016·2016-09-07

    Tippins Cream Cheese Pie Base Recalled for Potential Peanut Residue

    Tippin's Gourmet Pies is recalling 60 cases of 9-inch cream cheese pie bases because they may contain low levels of peanut residue.

    Product
    Tippins 9" Cream Cheese Base packaged in ?. UPC code is 680816002711. Packaged in 18 pie bases per case. Shipped frozen.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-2689-2016·2016-09-07

    Mindray A7 Anesthesia Delivery System Recalled for Potential Oxygen Leak

    Mindray is recalling 167 A7 Anesthesia Delivery Systems due to a potential leak on the back-up oxygen and air cylinder yokes.

    Product
    A7 Anesthesia Delivery System, a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. Part numbers 0632F-PA0000X (US domestic) and 0632B-00014 (international)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1994-2016·2016-09-07

    Tippin's Key Lime Pie Bases Recalled for Potential Peanut Residue

    Tippin's Gourmet Pies is recalling 8-inch Key Lime Pie Bases because they may contain low levels of peanut residue. The product was distributed to seven states.

    Product
    Tippins 8" Key Lime Base packaged in ?. UPC code is 680816001851. Packaged in 12 pie bases per case. Shipped frozen. Net wt. 21oz each.
    Category
    Food
    Distribution
    7 states
  • HighNHTSA·16C007000·2016-09-07

    Evenflo Recalls Evolve 3-in-1 Booster Seats Due to Harness Loosening Risk

    Evenflo is recalling specific Evolve 3-in-1 Combination Booster Seats because children can access a button to loosen the harness, increasing injury risk in a crash.

    Product
    CHILD SEAT:HARNESS:STRAP/WEBBING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide