State
72,820 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 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Stryker is recalling Hoffmann II Connecting Rod Micro 3 x 30mm (catalog 50796030) because the rods may crack after cleaning and sterilization. FDA has classified this as Class II.
Windstone Medical Packaging is recalling 100 AMS convenience kits labeled Block Tray - RX, Part Number AMS12414, because they contain Elevaris Lidocaine HCl injection recalled for supplier quality issues.
Windstone Medical Packaging is recalling specific AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP due to supplier quality issues.
Windstone Medical Packaging is recalling specific AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP due to supplier quality issues.
Terex Utilities is recalling Power Over Fiber Base Modules because the devices lack proper laser certification and contain incorrect safety labeling regarding their laser class.
Windstone Medical Packaging is recalling 3,378 AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP because the lidocaine was recalled due to supplier quality issues.
Windstone Medical Packaging is recalling 24 AMS Heart Cath Tray convenience kits containing Elevaris Lidocaine HCl injection because the lidocaine was recalled for supplier quality issues.
Glenmark Pharmaceuticals is recalling azelaic acid gel 15% after receiving complaints that the product felt grainy, gritty, or sandy. The nationwide recall covers specific lots with expiration dates from February through April 2028.
Windstone Medical Packaging is recalling 60 AMS Angio Pack-RX convenience kits (lots 230658, 231173) because the included Elevaris Lidocaine HCl injection was recalled by its manufacturer due to supplier quality issues.
Ascend Laboratories is recalling dabigatran etexilate capsules due to an out-of-specification result in related substance testing involving Impurity II, Impurity III, and total impurities observed during 12-month stability testing.
Ascend Laboratories, LLC is recalling Dabigatran Etexilate Capsules (150 mg) because testing showed impurities exceeded established limits during stability testing.
Ascend Laboratories, LLC is recalling Dabigatran Etexilate Capsules (75 mg) because testing showed impurities exceeded established limits during stability testing.
Escape Trailer Industries is recalling 2025-2026 E13 F1 recreational trailers because insufficient refrigerator ventilation may allow carbon monoxide to build up inside the cabin.
Tesla, Inc. is recalling certain 2017-2023 Model 3 and 2020-2023 Model Y vehicles because the headlight low beams may be too bright, increasing the risk of a crash.
Wabash is recalling 2027 Van Trailers because the external ABS malfunction indicator light may lack a label, potentially confusing other drivers.
Daimler Trucks North America is recalling aftermarket Grote Headlamps because a software error may cause low beams to illuminate improperly, increasing crash risk.
Forest River is recalling 2027 Freelander and Leprechaun recreational vehicles because a missing breaker leaves the power feed wire without overcurrent protection, increasing fire risk.
Rosenbauer is recalling certain 2024-2026 emergency vehicles because a display unit may fail, preventing the activation of exterior lights and firefighting equipment.
Alamo Group is recalling 2022-2026 Royal Truck & Equipment Class 2 Traffic Control trucks because solar panel screws may loosen, causing the panel to detach and strike others.
About 121,680 Galanz retro-style refrigerators can short circuit and ignite. CPSC is aware of 34 fire reports, one of which resulted in a fatality. Free in-home repair is offered.
About 1.5 million OCOOPA lithium-ion hand warmers can overheat and ignite. The firm reports 1,480 overheating incidents, 15 fires and 350 burn injuries, including the death of an 83-year-old consumer.
General Motors is recalling certain 2026 Cadillac Escalade, GMC Sierra EV, and Chevrolet Silverado EV models because an improperly secured battery component may increase the risk of a fire.
TT Trsmima backyard zipline kits and spring brakes can break, detach or fail to slow riders. Reports include fractures, concussions, sprains and abrasions across two separate failure modes.
Honda is recalling certain CMX300, CMX500, and SCL500 motorcycles because the handlebar lock screw may loosen and detach, potentially interfering with steering.
Winnebago is recalling certain 2024-2025 Ekko motorhomes because the touchscreen display may register unintended inputs and turn the generator on without the operator's knowledge.