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.
Blue Bird is recalling 2026-2027 Vision and All American school buses because wheelchair restraints may fail to lock, increasing injury risk.
Philips North America is recalling the IntelliVue Patient Monitor MX100 over a potential issue where the monitors did not alarm.
Breckenridge Pharmaceutical is recalling 7,389 bottles of Duloxetine Delayed-Release Capsules, 60 mg, over the presence of N-nitroso-duloxetine above the FDA recommended limit.
Philips North America is recalling the IntelliVue MP80 over a potential issue where the monitors did not alarm.
Volkswagen is recalling 3,138 model year 2025 Tiguan vehicles because a fault in the passenger occupant detection system wiring may deactivate the front passenger air bag when the seat is occupied.
Philips North America is recalling the IntelliVue Patient Monitor MX600 over a potential issue where the monitors did not alarm.
Motor Coach Industries is recalling various transit bus models because the front door lower curb view glazing material is incorrect, which may reduce driver visibility and increase crash risk.
Paragon 28 is recalling 20 Phantom Fibula Nails because out of specification thread depths may prevent the implant from mating with its mounting bolt, potentially requiring surgery to be aborted.
Costco is recalling 612 retail units of Kirkland Signature Chicken Sandwich with Caesar Salad because the 3 oz sealed packet of Caesar dressing may contain plastic material.
Costco is recalling 142,532 retail units of Kirkland Signature Caesar Salad because the 3 oz sealed packet of Caesar dressing may contain plastic material.
Hale inc is recalling 54 bottles of Lotsa Pasta Roasted Garlic Infused Olive Oil over the potential for Clostridium botulinum contamination.
Philips North America is recalling the IntelliVue Patient Monitor MX400 over a potential issue where the monitors did not alarm.
Blue Bird is recalling 2025-2027 Vision school buses because a missing support brace may cause the wheelchair lift to fail, increasing injury risk.
Philips North America is recalling the IntelliVue MP50 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP70 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP90 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP2 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX850 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX550 over a potential issue where the monitors did not alarm.
Medtronic is recalling 6,591 Aurora EV-ICD and Clinical EV-ICD single chamber extravascular defibrillators over the potential for delayed time to high-voltage therapy in a rare sequence of events.
Philips North America is recalling the IntelliVue Patient Monitor MX750 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX450 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX700 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP40 over a potential issue where the monitors did not alarm.
Breckenridge Pharmaceutical is recalling 3,397 bottles of Duloxetine Delayed-Release Capsules, 60 mg, over the presence of N-nitroso-duloxetine above the FDA recommended limit.