State
72,940 recalls have nationwide distribution and so reach Missouri. 8,461 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,461 recalls naming Missouri we have scored against our rubric, 1,333 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,870 (22%) are Severe.
Which agencies issued them
These figures cover only the 8,461 recalls whose distribution notice names Missouri specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Rivian is recalling certain 2022-2025 R1T and 2022-2026 R1S vehicles because the bolts securing the second-row seat belt retractor assemblies may be improperly tightened.
About 330,000 Curtis International Frigidaire-brand 6-can minifridges, model EFMIS121, are being recalled after at least six reports of fires with property damage.
Ford is recalling 2013-2019 Focus, Escape, and 2015-2016 MKC vehicles because a cracked engine block heater may short circuit and cause a fire.
About 4,100 Energizer Large Power Indicator Lanterns are being recalled because the lithium-ion batteries installed in them can overheat, posing a burn hazard.
About 1,320 HEZI brand power strips are being recalled because they have an ungrounded metal enclosure that poses an electrocution hazard if energized.
About 1,260 Greatale self-feeding pillows are being recalled because they hold a bottle at an unsafe angle and fixed in place, which can lead to aspiration of milk or formula.
Gulf Stream is recalling 2026 Trail Boss and Ameri-Lite trailers because reversed taillight wires may cause turn signals to activate in the wrong direction.
About 1,500 KEAWIS crib mattresses are being recalled because they may not adequately fit certain play yards or non-full-sized cribs, creating gaps that pose an entrapment hazard.
Ford is recalling certain 2016-2018 Focus, 2019 Explorer and 2024 Explorer vehicles because the engine block heater may crack and develop a coolant leak, causing a short circuit when plugged in.
About 170 R.X.Y adult bike helmets are being recalled because they do not comply with impact attenuation, positional stability, labeling and certification requirements.
About 11,900 BBWOO baby loungers are being recalled because the sides are too low, the foot openings are too wide, and the loungers have no stand.
About 16,900 RootStim Beard Growth Serum bottles are being recalled because the serum contains minoxidil and the packaging is not child-resistant.
About 95 Morgan Lane Asher Pajama Sets, Style 816TR in Petal, are being recalled because they violate the mandatory flammability standards for children's sleepwear.
About 6,100 Adams RealComfort and StyleWell Adirondack patio chairs are being recalled because the chairs can crack and collapse, posing injury and fall hazards.
About 25,000 Ruahouine Hair Growth Serum bottles are being recalled because the serum contains minoxidil and the packaging is not child-resistant.
MediNatura is recalling all lots within expiry of ReBoost Nasal Spray after the products were found to contain yeast, mold and microbial contamination identified as Achromobacter.
MediNatura is recalling all lots within expiry of ClearLife Allergy Nasal Spray, Extra Strength, after the products were found to contain yeast, mold and Achromobacter.
AVID Medical is recalling 132 Halyard Organ Recovery OR Packs, kit code LLOG1000-15, because the devices are not suitable for organ transplant.
AVID Medical is recalling 52 Halyard Organ Recovery OR Packs because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.
AVID Medical is recalling 380 Halyard Mini Plus Kit South units because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.
Medline is recalling 1,611,081 Hudson RCI medium concentration oxygen masks after multiple complaints of tubing disconnecting, which may lead to shortness of breath and hypoxia.
MAYEJ Comercializadora is recalling 1,288 boxes of Italian Parsley over the pathogen Cyclospora cayetanensis.
Remote Diagnostic Technologies is recalling 7,129 Philips Tempus Pro Patient Monitors because intracranial and bladder pressure measurements have not been tested or validated for accuracy.
Town Food Service Equipment is recalling approximately 11,300 aluminum sauce pans in 1QT to 3QT sizes after the product was found to contain leachable lead levels.
Securitas Healthcare is recalling 1,898 Arial 900 MHz Call Stations, model CSK200-900MR, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.