State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
BioLite is recalling BaseLanterns and BaseLantern XLs because the lithium-ion batteries can overheat and catch fire. One report of minor property damage has been received.
VistaPharm is recalling Lactulose Solution, USP, 10 g/15 mL, because bulk solution tested positive for Burkholderia cepacia bacteria.
Pfizer is voluntarily recalling 2,666 bottles of LEVOXYL (levothyroxine sodium) 200 mcg tablets nationwide because the product is superpotent.
Merit Medical Systems is voluntarily recalling 178 Fluid Management Sets due to a compromised sterile barrier.
Merit Medical Systems is recalling 53 Procedure Kits due to a compromised sterile barrier. The kits were distributed nationwide to specific states and Japan.
CSC Motorcycles is recalling 2015-2016 Cyclone motorcycles because they may lack a required label reminding users to use DOT 4 brake fluid.
Hologic is recalling SURESOUND22 uterine sound multipacks because a breach in the sterile barrier compromises product sterility.
EN-R-G Foods is recalling Cherry Lime, Raspberry, and Juneberry Protein Chews due to consumer complaints of nausea and vomiting after consumption.
Merit Medical Systems is recalling 40 Manifold Kits (Catalog No. K09-11867AP) because the sterile barrier is compromised, posing a risk of infection.
Merit Medical Systems is voluntarily recalling 130 MeriTrans Pressure Monitoring Kits because a compromised sterile barrier may affect product sterility.
IMUSA is recalling about 17,500 espresso makers because the filler cap can crack or pop off, posing burn and impact risks.
Toshiba American Medical Systems is recalling Aquilion Prime CT systems because cooling oil in the x-ray tube heat exchanger may leak during operation.
Cummins is recalling 164 model year 2015-2016 generator sets because door hinges may fail, causing doors to detach and create road hazards.
Philips is recalling 1,363 CT scanners because the patient support tabletop may fail to move horizontally during scans due to a mechanical linkage failure.
LGS Industries is recalling 2017 Pace, Cargo Express, and Look cargo trailers because a defective weld could cause the ramp door bracket to detach, creating a crushing hazard.
EN-R-G Foods is recalling Cherry Lime Protein Chews due to consumer complaints of nausea and vomiting after consumption.
Merit Medical Systems is voluntarily recalling specific Procedure Kits due to a compromised sterile barrier, which may affect the sterility of the contents.
Siemens is recalling Dimension Vista Chemistry 1 Calibrators (lots 5GM081 and 5GM082) because they may cause discrepant low calcium recovery in quality control and patient samples.
Bausch + Lomb is recalling PeroxiClear Peroxide Solution because the product was found to contain excess residual levels of hydrogen peroxide.
EN-R-G Foods is recalling specific protein chew products due to consumer complaints of nausea and vomiting after consumption.
DiaSorin is recalling the LIAISON Estradiol II Gen assay because it may produce inaccurate results for patients treated with fulvestrant.
Philips is recalling 1,363 CT scanners because the patient support tabletop may fail to move horizontally during scans due to a mechanical linkage failure.
Summit Treestands is recalling about 270 Explorer SD closed front climbing treestands because a weld in the frame can break, posing a fall hazard.
Kia is recalling 2016-2017 Sorento and 2017 Sportage vehicles because a trailer hitch wiring malfunction may cause brake lights to stay on, confusing other drivers.
Merge Healthcare is recalling RadSuite software versions 8.30.7.8 through 8.31 because images may not appear readable, potentially delaying care or causing patient re-exposure to radiation.