State
72,940 recalls have nationwide distribution and so reach Iowa. 5,581 additional recalls listed Iowa specifically in their distribution scope.
Of the 5,581 recalls naming Iowa we have scored against our rubric, 909 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,317 (24%) are Severe.
Which agencies issued them
These figures cover only the 5,581 recalls whose distribution notice names Iowa specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Lucid is recalling certain 2022-2026 Air vehicles with the AD02 package on software versions 2.8.0 through 2.8.16, because the rearview camera image may not display when the vehicle is in reverse.
Lippert is recalling certain bus windows that may have illegible DOT markings, failing to comply with Federal Motor Vehicle Safety Standard 205.
Ford is recalling specific engine block heaters for 2013-2019 Ford and Lincoln vehicles because they may crack, leak coolant, and cause electrical short circuits that increase fire risk.
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.
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 330,000 Curtis International Frigidaire-brand 6-can minifridges, model EFMIS121, are being recalled after at least six reports of fires with property damage.
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.
About 25,000 Ruahouine Hair Growth Serum bottles are being recalled because the serum contains minoxidil and the packaging is not child-resistant.
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.
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 1,320 HEZI brand power strips are being recalled because they have an ungrounded metal enclosure that poses an electrocution hazard if energized.
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 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 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 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 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.
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 16,900 RootStim Beard Growth Serum bottles are being recalled because the serum contains minoxidil and the packaging is not child-resistant.
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.
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.
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.
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.
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.
MAYEJ Comercializadora is recalling 1,288 boxes of Italian Parsley over the pathogen Cyclospora cayetanensis.