State
72,940 recalls have nationwide distribution and so reach Minnesota. 7,804 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,804 recalls naming Minnesota we have scored against our rubric, 1,125 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,892 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,804 recalls whose distribution notice names Minnesota specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
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 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 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 16,900 RootStim Beard Growth Serum bottles are being recalled because the serum contains minoxidil and the packaging is not child-resistant.
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.
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.
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 25,000 Ruahouine Hair 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.
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 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 132 Halyard Organ Recovery OR Packs, kit code LLOG1000-15, because the devices are not suitable for organ transplant.
Lund Food Holdings is recalling 108 cases of Lunds & Byerlys Monster Cookies over undeclared peanut, egg and soy. The FDA has classified the action as Class I.
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.
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.
MAYEJ Comercializadora is recalling 1,288 boxes of Italian Parsley over the pathogen Cyclospora cayetanensis.
Philips North America is recalling 13,470 Smart-hopping 2.0 AP 1.4 GHz patient monitors because the MX40 could not reconnect to the PIC iX when signal strength changed quickly.
IMRIS Imaging is recalling 122 HFD100 Head Fixation Devices because a torque screw may crack or separate, which could lead to inadequate head stabilization and risk of patient injury.
Meridian Bioscience is recalling 211 units of the Revogene C. difficile assay because affected lots show a decline in performance over time, which may lead to false-negative results.
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.
McCain Foods USA is recalling 21,256 cases of Ore-Ida Tater Tots shaped potatoes over clear hard plastic fragments.
CareFusion 303 is recalling 2,079 BD Pyxis ES Enterprise Server systems over a software issue that may result in equipment not receiving timely updates of patient or medication information.
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.
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.
Imprimis NJOF is recalling 596 boxes containing 11,920 pre-filled syringes of Dexamethasone, Moxifloxacin and Ketorolac intraocular injection over glass-like particles.