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.
Waymo is recalling 3,067 5th Generation Automated Driving Systems because software may cause vehicles to pass stopped school buses, increasing crash risk.
Ducati is recalling 2025-2026 Panigale V2 and Streetfighter V2 motorcycles because reversed fuses may cause ABS malfunction and wheel lockup.
Micro Bird is recalling 2022-2026 G5 and T-Series transit buses because a loose power cable connection may cause the air conditioning control board to overheat and melt, increasing the risk of a fire.
Micro Bird is recalling 2021-2026 G5, T-Series, and MB II school buses because a loose power cable connection may cause the air conditioning control board to overheat and melt, increasing the risk of a fire.
About 210,000 INIU 10,000mAh power banks, model BI-B41, are being recalled after 15 reports of overheating including 11 fires, three minor burn injuries and over $380,000 in property damage.
Nova Bus is recalling certain water pumps because a loose impeller shaft may cause pump failure, increasing crash risk.
Motorcar Parts of America is recalling specific brake calipers for 2008-2025 Ford E-450 Super Duty vehicles because the piston bore wall may not meet specifications, causing the caliper to fracture.
About 250 FUFU&GAGA queen size Murphy wall beds are being recalled after two reports of the 215-pound frame falling during assembly, injuring two consumers.
About 3,170 Primark Water Balloon Pumps are being recalled because they can generate excessive pressure and rupture. Two US reports of cuts to hands and fingers have been received.
About 40 Cubimana treehouse building toy sets are being recalled because button cell batteries in the LED light piece can be easily accessed by children.
About 10,380 KTEBO writing tablet toys are being recalled because the screw securing the button cell battery compartment does not remain attached as the mandatory toy standard requires.
About 300 Little Pea Shop padded crib bumpers are being recalled because they can obstruct an infant's breathing and are banned under the Safe Sleep for Babies Act.
About 4,120 Casaottima 13-Drawer Dressers are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act standard.
About 9,400 CreateOn Crayola-branded pip-Cubes are being recalled because magnets can come loose if the seams separate, posing an ingestion hazard to children.
About 2,300 Grizzly Industrial 15-inch 3HP heavy-duty planers, model G0815, are being recalled because the chip breaker can contact the cutterhead blades and eject debris.
BMW is recalling 2026 X6, X7, X5, and X5 Plug-In Hybrid models. The instrument panel may prevent the passenger-side airbag from deploying properly during a crash.
About 17,000 HydroJug 14-ounce children's sport tumblers are being recalled because the rivets on the handle can come loose, causing the handle to detach and posing a choking hazard.
Fresenius Kabi is recalling 2,199,850 vials of Famotidine Injection USP after out of limit results were obtained for endotoxin testing. The FDA classified it Class I.
Olympus is recalling 7,023 EVIS EXERA III TJF-Q190V duodenovideoscopes after continued reports of positive cultures and infections, and is updating the reprocessing materials.
Medtronic Sofamor Danek is recalling 275,260 Catalyft PL and PL40 expandable interbody spacers because the cage may lose height or collapse, risking migration or neurological injury.
Intelerad Medical Systems is recalling 19 IntelePACS InteleConnect and TechPortal installations because a bug can cause data loss in the Relevant Clinical Info field.
B. Braun Medical is recalling 23,160 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.
Straumann USA is recalling 61 units of Emdogain because product intended for demonstration purposes only could be placed in patients.
Magellan Diagnostics is recalling 1,774 LeadCare II Blood Lead Test Kits because calibration buttons used in kitting were labelled with the wrong lot number.
Volkswagen is recalling approximately 629 2023-2024 ID.4 vehicles with defective high-voltage battery cell modules. Misaligned electrodes in the battery may cause fires, posing a risk of injury to vehicle occupants.