State
73,817 recalls have nationwide distribution and so reach Missouri. 8,501 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,501 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 2,204 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
E-One is recalling 2001-2002 X-036 and X-113 emergency vehicles because fire pump manifold end caps may fail, causing sudden water discharge or pressure loss.
E-One is recalling 2013-2017 Quest II, Cyclone II, and Typhoon emergency vehicles because a missing diode may damage the starter lock-out relay, preventing the vehicle from starting.
Skip Hop is recalling Tuo convertible high chairs because the front legs can detach, posing a fall hazard to children.
Jaguar Land Rover is recalling 2009-2010 Range Rovers because the passenger air bag inflator may explode during deployment, potentially causing serious injury or death.
Jaguar Land Rover is recalling 2010-2012 Range Rovers because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Jaguar is recalling 2010-2015 XF vehicles because the front passenger air bag inflator may explode during deployment, potentially causing serious injury or death.
Jaguar is recalling 2009-2013 XF vehicles because the front passenger air bag inflators may explode during a crash, potentially causing serious injury or death.
Terex is recalling 2015-2017 XT Pro 56 and 60 aerial devices because the platform control enable system may be adjusted incorrectly, increasing injury risk.
McLaren is recalling 371 2013 MP4-12C vehicles because the passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Crescent City Meats is recalling approximately 430 pounds of ready-to-eat Tasso Cajun Spicy Ham because the product may be underprocessed and undercooked.
HP is recalling about 50,000 lithium-ion batteries for notebook computers and mobile workstations because they can overheat, posing fire and burn hazards.
Volkswagen Group of America is recalling specific Audi models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Gulf Stream is recalling 2011-2012 recreational trailers because the installed fire extinguishers may clog or detach, potentially failing to discharge or causing injury.
Altec Industries is recalling 2010-2011 Effer 440 and 470 Knuckle Boom Cranes because rotation bearing fasteners may fail, causing the pedestal to crack and increasing injury risk.
SureFit is recalling about 900 riding lawn mower blade spindle shafts and assemblies because they can break and become projectiles, posing an impact injury risk.
Sterilmed Inc is recalling 112 reprocessed St. Jude Medical Agilis NxT Steerable Introducers due to inadequate seals caused by missing adhesive glue.
SSM St. Clare Health Center is recalling compounded phenylephrine syringes because microbial growth was detected during a routine manufacturing simulation. No distributed product has been confirmed to contain microorganisms.
SSM St. Clare Health Center is recalling specific lots of compounded Oxytocin IV bags due to a lack of sterility assurance. No distributed product has been identified as actually containing microorganisms.
Forest River is recalling 2018 Glaval Legacy buses because improperly tightened brake caliper bolts may cause the calipers to detach, reducing braking power and increasing crash risk.
L3 Security & Detection is recalling 471 Examiner 3DX 6000 cabinet X-ray systems used for airline baggage screening due to shielding gaps that may cause excessive X-ray emissions.
SSM St. Clare Health Center is recalling compounded fentanyl and ropivacaine injectable bags due to a lack of sterility assurance. Microbial growth was detected during a routine simulation, though no distributed product was found to contain microorganisms.
SSM St. Clare Health Center is recalling specific lots of compounded Norepinephrine IV bags in Missouri due to microbial growth detected during a routine manufacturing simulation.
Philips is recalling specific IntelliVue patient monitors and measurement servers because they may display distorted ST-segments during 12-lead ECG monitoring.
Medline Industries is recalling 5,722 units of sterile elastic bandages because they may not have been properly sterilized.
SSM St. Clare Health Center is recalling compounded Neostigmine Methylsulfate syringes because microbial growth was detected during a routine manufacturing simulation. No distributed product has been confirmed to contain microorganisms.