State
72,940 recalls have nationwide distribution and so reach Oklahoma. 5,788 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,788 recalls naming Oklahoma we have scored against our rubric, 1,033 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,238 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,788 recalls whose distribution notice names Oklahoma specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Moonlight Packing is recalling 439 bags of 4-count Peppermint Peach packs over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
ByHeart is recalling 3,482,131 cans and 3,531,901 single serve packets of Whole Nutrition Infant Formula after contamination with Clostridium botulinum. The FDA has classified the action as Class I.
Moonlight Packing is recalling 2,603 cases of loose bulk peppermint peaches over potential contamination with Listeria monocytogenes, under enforcement record H-0323-2026.
Chetak New York is recalling Deep-brand frozen sambhar mix after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Moonlight Packing is recalling 483,973 cases of 4 lb packaged yellow peaches over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Moonlight Packing is recalling 104 cases of 2 lb bagged white peaches over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Moonlight Packing is recalling 570 cases of 2 lb Peppermint Peach bags over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Autocar is recalling one 2024 E-ACTT terminal tractor because improperly secured battery cable connections may overheat and cause a fire or loss of motive power.
BMW is recalling specific 2014-2015 2, 3, and 4 Series vehicles because the head air bag inflator may fail, posing an injury risk during a crash.
Toyota is recalling certain 2024-2025 Highlander and Highlander Hybrid vehicles because the third row centre seat belt roof anchor may have been installed at an incorrect angle.
Suzuki is recalling 2025-2026 DR-Z400S and 2025 DR-Z400SM motorcycles because incorrectly tightened screws may allow brake fluid to leak, reducing braking ability.
Rollx Vans is recalling certain converted vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints, because the retractors may not lock and the wheelchair may not be properly secured.
Medline is recalling 15 Medline Perfusion Syringes because they contain BD Luer Tip Caps from trays that failed routine biocompatibility testing.
Vantage Mobility is recalling 2021–2025 Chrysler Pacifica vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints because the retractors may fail to lock, allowing wheelchairs to move unsecured during transit.
Cipla USA is recalling 63,504 bottles of Cinacalcet Hydrochloride Tablets, 30 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.
Bard Peripheral Vascular is recalling 1,240 Safe-T-Centesis 6 Fr Catheter Drainage Trays because the safety indicator can show the catheter in the sharp position when it is blunt.
Bell Sports is recalling Scout Air helmets in sizes S and L because they may lack proper penetration protection, failing federal safety standards.
JR Simplot is recalling 7,053 cases of Simplot Traditional Reduced Sodium Tater Gems after pieces of semi-rigid plastic were found embedded in the product.
Kia is recalling certain 2023-2025 Sportage and Sportage Plug-In Hybrid vehicles with a 4.2-inch screen and a Kia tow hitch harness, because a software error may make the instrument panel screen fail.
Cipla USA is recalling 12,576 bottles of Cinacalcet Hydrochloride Tablets, 90 mg, over the presence of N-nitroso-cinacalcet above the acceptable daily intake limits.
Dr. Reddy's Laboratories is recalling 4,800 bottles of Varenicline Tablets, 1mg, after the assay value for the affected lot fell below the specification limit at nine-month stability testing.
Orthofix U.S. is recalling 13,317 Pillar SA PTC Spacer System units because the labeling contains claims that are not consistently present.
Orthofix U.S. is recalling 40,956 CONSTRUX Mini Ti Spacer System units because the labeling contains claims that are not consistently present.
Orthofix U.S. is recalling 61,977 CONSTRUX Mini PTC Spacer System units because the labeling contains claims that are not consistently present.
Cipla USA is recalling 1,180 boxes of Lanthanum Carbonate chewable tablets, 1000mg, from a further lot after an out of specification hardness test result.