State
73,366 recalls have nationwide distribution and so reach Oklahoma. 5,816 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,816 recalls naming Oklahoma we have scored against our rubric, 1,043 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,490 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,816 recalls whose distribution notice names Oklahoma specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Catalina Snacks is recalling Spicy Kick ready-to-eat snack mix pouches due to potential metal contamination. The product was distributed across multiple U.S. states and online sales.
Celestial Seasonings Mandarin Orange Spice herbal tea K-cups contain undeclared caffeine from black tea. The recall affects 1,844 units distributed nationwide.
Scientia Vascular is recalling Plato 17 Microcatheters due to manufacturing defects that may introduce loose particles into the catheter lumen, potentially causing blood vessel blockage or inflammatory reactions.
Fenwal Inc is recalling 6,564 units in certain lots of Amicus apheresis kits because centrifuge packs may develop a stress leak. No illnesses or injuries have been reported.
Securitas Healthcare is recalling the Arial mobile application for Android devices because the app does not load or function properly. Users should stop using the app immediately.
Catalina Snacks is recalling Chocolate Peanut Butter cereal (9oz pouches) due to metal contamination. The recall affects approximately 316,980 pouches distributed across multiple states and online retailers.
Breckenridge Pharmaceutical is recalling Clobazam 20 mg tablets (Lot #5210147, exp. 12/2023) nationwide due to potential cross contamination from manufacturing deviations.
Catalina Snacks is recalling Maple Waffle flavored ready-to-eat cereal due to the potential presence of metal fragments. Consumers should not consume the affected product.
Volvo is recalling 2023 S60, C40, XC40, V60CC, XC60, and XC90 vehicles because a false warning may mask an actual emergency call system failure.
Intuitive Surgical recalls Patient Side Carts for da Vinci X and Xi surgical systems due to ballscrew failure risk. The failure could cause uncontrolled carriage movement leading to potential tissue injury during surgery. 9 units affected.
Alexis Fire Equipment is recalling 2022 fire apparatus vehicles because water may enter the winch remote, causing corrosion and unintentional winch operation.
Catalina Snacks is recalling fruit flavored ready-to-eat cereal in 1.27 oz and 8 oz pouches due to potential metal foreign material contamination. Consumers who purchased affected products should not consume them.
Becton Dickinson & Company is recalling 1.17 million BD Ultra-Fine Insulin Syringes due to a nonsterile manufacturing defect that could expose patients to pathogenic microorganisms and increase infection risk.
OMM Imports' Recreo Hair Growth Laser Comb is being recalled because 1,620 units lack required safety labels, warnings, and certification documentation. Missing labels create risk for users of the Class 3R laser device.
Brainlab ExacTrac Dynamic software used in charged-particle radiation therapy systems may not properly execute Deep Inspiration Breath Hold (DIBH) functionality, a heart-protection technique. The issue affects 56 systems across the United States.
Stryker's Power-PRO 2 ambulance cots may separate at head or foot due to insufficient epoxy. Four affected units in NY and VA should be removed from service immediately.
Bard Peripheral Vascular is recalling certain Bard Mission Disposable Core Biopsy Instrument Kits due to sizing incompatibility between the biopsy instrument and coaxial needle, which could cause procedural delays or needle breakage.
BD Insulin Syringes (Catalog 329420) are being recalled due to nonsterile conditions that could expose patients to pathogenic microorganisms and increase infection risk. The recall affects 961,000 units distributed worldwide.
Navada Imports is recalling 575 cases of soybean lecithin powder due to undeclared peanut allergen. Affected products were distributed nationwide to manufacturers.
Navada Imports is recalling sunflower lecithin powder in 44 lb. boxes due to an undeclared peanut allergen. The affected product poses a serious risk to consumers with peanut allergies.
BioFire Diagnostics is recalling BioFire BCID2 diagnostic panels that experienced temperature excursions during shipment, which may reduce their performance. Affected kits were distributed in Florida and Georgia.
Breckenridge Pharmaceuticals is recalling certain lots of Clobazam 10 mg tablets due to a potential cross-contamination risk stemming from manufacturing process deviations.
BioFire Diagnostics is recalling BioFire Respiratory Panel 2.1 (RP2.1) diagnostic kits due to temperature excursions during shipping that may reduce device performance.
BioFire Diagnostics is recalling FilmArray GI Panel diagnostic kits due to temperature excursions during shipping that may reduce test performance.
Navada Imports is recalling Organic Sunflower Lecithin Powder (44 lb boxes) due to undeclared peanut allergen. The product was distributed to a distributor in Missouri and then nationwide to manufacturers.