State
72,940 recalls have nationwide distribution and so reach DC. 2,795 additional recalls listed District of Columbia specifically in their distribution scope.
Of the 2,795 recalls naming District of Columbia we have scored against our rubric, 240 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 946 (34%) are Severe.
Which agencies issued them
These figures cover only the 2,795 recalls whose distribution notice names District of Columbia specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 9,300 Joyful Journeys baby loungers are being recalled because the sides are too low, the foot openings are too wide, and the loungers have no stand.
About 1,200 PNW Components Loam Pedal Gen 2 mountain bike pedals are being recalled because the pedal axle can crack, causing the pedal to detach from the crank.
About 280 BabyBond retractable safety gates are being recalled because a child's torso can fit through the opening between the gate and the floor and become entrapped.
About 2,240 Kori Gey water elf toy kits are being recalled because the button cell battery compartment can be easily accessed and opened by children.
About 13,200 Isla Rae magnetic wireless chargers are being recalled because the chargers can explode while in use, posing fire and burn hazards.
About 26,200 Sangohe adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and the mattress.
Wanli Tire Corporation is recalling Aptany Eco Sendero M/T2 tires because the sidewall may separate, increasing the risk of a crash.
Tom Bumble is recalling approximately 6,500 units of Nutty Peanut Butter Flake Candy with Peanut & Chocolate over foreign material.
Sheathing Technologies is recalling 12 units of Sheathes3D vaginal and rectal ultrasound probe covers because product defects may result in contamination during use, posing an infection risk.
Novo Nordisk is recalling Wegovy (semaglutide) Injection, 1 mg/0.5 mL prefilled pens, over the presence of particulate matter after hair was found in a prefilled syringe.
Novo Nordisk is recalling Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL prefilled pens, over the presence of particulate matter after hair was found in a prefilled syringe.
CareFusion 213 is recalling 106,400 units of BD ChloraPrep Triple Swabsticks over a lack of assurance of sterility.
Glenmark Pharmaceuticals is recalling 96,948 packs of Ondansetron Orally Disintegrating Tablets, 4mg, because the blister packs are not fully sealed and tablets are falling out.
Ferndale Laboratories is recalling 24,589 units of Mastisol Liquid Adhesive because the butyrate tube cracks during actuation, rendering the product unusable.
Philips Ultrasound is recalling 1,721 EPIQ Ultrasound Systems used with the X5-1c transducer because the system may experience an unexpected automatic reboot, resulting in damage to the transducer.
Beaver-Visitec International is recalling 5 BVI Leos Laser and Endoscopy Systems because ferrites specified for the USB cable assembly were not installed as intended.
Zydus Pharmaceuticals is recalling 2,136 bottles of traZODONE Hydrochloride Tablets, 100mg, after a product complaint that some tablets had a dent on the plain side of the tablet surface.
Blue Bird is recalling 2026 Vision and All American electric transit buses because wheelchair restraints may fail to lock, increasing injury risk.
Rivian is recalling certain 2022-2025 R1S and R1T vehicles that previously had service performed, because the toe link may have been reassembled incorrectly and the joint may separate.
Blue Bird is recalling 2022-2024 All American electric transit buses because a loose 12-volt cable may disconnect, causing loss of electrical systems and increasing crash risk.
Allwin Powersports is recalling specific LS2 Rebellion helmets that may lack proper impact protection, increasing the risk of injury during a crash.
Volvo Car USA is recalling 40 model year 2025 EX30 vehicles because the high-voltage battery may experience a short circuit and overheat, increasing fire risk.
Alcon Research is recalling 151 Custom Pak ophthalmic procedure packs because the packs may have incomplete seals affecting sterility. The FDA has classified the action as Class I.
Draeger is recalling 431 Vapor 2000 anesthetic vaporizers because a certain component was not delivered within specification and contained impurities. The action is Class I.
Draeger is recalling 188 Vapor 3000 anesthetic vaporizers because a certain component was not delivered within specification and contained impurities. The action is Class I.