State
72,940 recalls have nationwide distribution and so reach Mississippi. 5,349 additional recalls listed Mississippi specifically in their distribution scope.
Of the 5,349 recalls naming Mississippi we have scored against our rubric, 923 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,126 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,349 recalls whose distribution notice names Mississippi specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
USDA FSIS issued a public health alert for FreshRealm ready-to-eat meals containing riced cauliflower that may be contaminated with Listeria monocytogenes.
Lucid is recalling 2022-2025 Air vehicles due to a software defect that may prevent the rearview camera from displaying or show inaccurate images, increasing crash risk. A free over-the-air software update will be provided.
USDA FSIS issued a public health alert for FreshRealm ready-to-eat meals containing spinach recalled for possible Listeria contamination. No illnesses have been reported.
Chrysler is recalling certain 2024–2025 RAM ProMaster battery electric vehicles due to software issues in the electric drive module that may cause loss of drive power, increasing crash risk.
Mack is recalling certain 2019-2025 MD, Anthem, Granite, and 2024 MD Electric and 2025 Pinnacle trucks with passenger bench seats. An improperly welded seat belt anchorage bracket may detach during a crash, increasing injury risk.
Foster Poultry Farms is recalling chicken corn dogs and ground turkey on a stick products due to possible wood contamination. Consumers should not eat these items.
Forest River is recalling 2025-2026 Entourage recreational vehicles because a suspension bolt may fail, causing the leaf spring to detach and increasing crash risk.
Altec is recalling 2024 FOSV-CA vehicles because an interconnect battery cable may overheat, increasing the risk of a fire.
Altec is recalling 2022-2025 ST600 vehicles with auxiliary engines because overloaded electrical circuits may overheat and increase the risk of fire.
REV is recalling 2024-2026 Fleetwood Fortis and Holiday Rambler Invicta RVs with theater seats because theater seat fasteners may have damaged propane hoses, creating a fire hazard.
Autocar is recalling 2023-2026 Legend and Xpeditor vehicles because the steering wheel nut may be improperly secured, allowing the wheel to separate from the column.
About 2,400 Kogalla power banks are being recalled after two reports of lithium-ion batteries overheating and catching fire, causing one minor burn injury and about $3,300 in property damage.
About 630 Blossom children's two-piece loungewear sets are being recalled because they violate the mandatory flammability standard for children's sleepwear.
About 470 Almpal dissolved oxygen test kits are being recalled because the sulfuric acid bottle inside is not in child-resistant packaging, as the Poison Prevention Packaging Act requires.
About 610 Gunaito 10-drawer dressers sold on Walmart.com are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act stability standard.
About 98,350 Evermore Surprise Eggs are being recalled because the toy airplane inside contains lead above the federal lead content ban. No incidents have been reported.
Hyundai is recalling 2024-2025 Santa Fe vehicles. The starter motor terminal cover may be improperly installed, causing electrical shorts that increase fire risk during crashes.
Toyota is recalling certain 2025 Tacoma and Tacoma Hybrid vehicles because the front driveshaft CV joint may deform and break, impairing steering and risking vehicle rollaway while parked.
Abiomed is recalling specific Automated Impella Controllers with defective Pump Driver Circuit Assemblies that may cause decreased pump performance or pump stop. The defect triggers Impella Failure or Impella Stopped Controller Failure alarms.
Vasoview Hemopro 3 Endoscopic Vessel Harvesting Systems are recalled after out-of-box failures including deformed jaw attachments, jaws not fully closed and lifted heater wire. 98 units are affected.
The Philips Allura Xper FD20/15 OR Table is recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. One unit is affected.
BeneVision N1 Patient Monitors are recalled because of the potential for activation of an abnormal alarm pause. 2,278 units are affected.
Philips IQon Spectral CT systems, model 728332, are recalled because the patient support table may descend unexpectedly due to ball screw misalignment after a replacement. 81 units are affected.
Voyant 1-Day Premium Toric contact lenses from one lot are recalled because the lot was manufactured with an invalid sterilization cycle. 90 units are affected.
Philips is recalling certain CT systems because the patient support table may descend unexpectedly to the lowest position due to a component misalignment during replacement.