State
73,741 recalls have nationwide distribution and so reach Missouri. 8,500 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,500 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,203 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,500 recalls whose distribution notice names Missouri specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Hank's Cheesecakes is recalling 207 banana cheesecakes because they lack labels indicating ingredients and major food allergens.
GE Healthcare is recalling 292 units of the Centricity Universal Viewer because it may fail to warn users when medical images are missing from exams.
Winnebago is recalling 2017-2019 Forza motorhomes because the exterior storage compartment door may unexpectedly open while driving, increasing crash risk.
Maquet is recalling 9 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, posing a risk of particles falling into the surgical field.
Maquet is recalling 7 units of VOLISTA StandOP Surgical Lights because the coating on the light head forks may crack, posing a risk of particles falling into the surgical field.
GE Healthcare is recalling ECG leadwire sets because they may reduce energy reaching patients during defibrillation, potentially limiting treatment success.
Just Love Fashion is recalling Prince of Sleep children's pajama pants because they fail federal flammability standards, posing a burn risk.
Hank's Cheesecakes, LLC is recalling 207 Chocolate Swirl Cheesecakes because they were distributed without labels indicating ingredients or major food allergens.
GE Healthcare is recalling 58,045 replacement ECG leadwires because they may reduce energy reaching patients during defibrillation, potentially limiting treatment success.
Hank's Cheesecakes is recalling Caramel Macchiato Cheesecakes because they lack labels indicating ingredients and major food allergens.
Maquet is recalling 65 VOLISTA StandOP Surgical Lights because the coating on the light head forks may crack, posing a risk of particles falling into the surgical field and causing patient infection.
Hank's Cheesecakes, LLC is recalling 207 chocolate cakes because they were distributed without labels indicating ingredients or major food allergens.
Maquet is recalling 10 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, potentially dropping particles into the surgical field.
Hank's Cheesecakes, LLC is recalling 207 Strawberry Cheesecakes distributed in Missouri and Illinois because they lack labels indicating ingredients and major food allergens.
Hank's Cheesecakes, LLC is recalling 207 unlabeled cheesecakes distributed in Missouri and Illinois because they lack ingredient and allergen labels.
Hank's Cheesecakes, LLC is recalling 207 Chocolate Amaretto Tortes because the packaging lacks ingredient and major food allergen information.
Maquet is recalling two VOLISTA StandOP Surgical Lights because the light head fork coating may crack, posing a risk of particles falling into the surgical field and causing patient infection.
Maquet is recalling five VOLISTA StandOP Surgical Lights because light head fork coatings may crack, posing a risk of particles falling into the surgical field.
Hank's Cheesecakes, LLC is recalling 207 White Chocolate Raspberry Cheesecakes because they were distributed without labels indicating ingredients or major food allergens.
Collins Aerospace is recalling 433 TASE 400 Imaging systems because the Nominal Ocular Hazard Distance for the alignment laser was miscalculated.
Hank's Cheesecakes, LLC is recalling 207 Triple Play Cakes because the packaging lacks ingredient and major food allergen information.
Hank's Cheesecakes, LLC is recalling 207 carrot cakes sold in Missouri and Illinois because the packaging lacks ingredient and allergen labels.
Maquet is recalling 11 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, posing a risk of particles falling into the surgical field.
AtriCure is recalling 497 units of the EPi-Sense Guided Coagulation System because the sterile package seal may be compromised, posing a risk of infection.
GE Healthcare is recalling Centricity PACS-IW with Universal Viewer version 5.0 because medical images may be missing without warning.