State
72,820 recalls have nationwide distribution and so reach Mississippi. 5,348 additional recalls listed Mississippi specifically in their distribution scope.
Of the 5,348 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 1,125 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,348 recalls whose distribution notice names Mississippi specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Winston Porter and Seeday 3-drawer, 4-drawer, and 5-drawer dressers are being recalled because they can tip over or cause entrapment, posing serious injury or death risks to children.
Jayco is recalling 2027 Eagle and Heartland Sundance fifth wheel trailers because auto leveling jacks may lower during transit, increasing crash risk.
Toyota is recalling 2026 bZ Woodland vehicles equipped with a tow converter due to an electrical short circuit risk that can disable stability control and keep brake lights on.
Chrysler (FCA US, LLC) is recalling certain 2023-2026 Alfa Romeo Tonale and 2023-2025 Dodge Hornet vehicles because the rear outboard seat belts may fail to retract properly.
Mack Trucks is recalling 2027 Anthem and Pioneer models because center roof marker lights may fail to illuminate, reducing visibility.
Evenflo is recalling Revolve180 Litemax NXT child seats manufactured through March 31, 2025, because a miscalibrated level indicator may cause the seat to sit too upright, increasing injury risk in a crash.
Toyota is recalling certain 2024 Tacoma hybrid and 2024-2025 Tacoma vehicles because their rear shock absorber assemblies may corrode and fail, potentially detaching the external oil reservoir and creating a road hazard.
Syera is recalling Space Astronaut LED Finger Lights sold on Temu because the button cell batteries can be easily accessed by children, posing a risk of serious injury or death if swallowed.
Volvo Trucks is recalling 2026-2027 VNL and VNR models because center roof marker lights may fail to illuminate, reducing visibility.
OKK Trading, Inc. is recalling three models of Easter LED Headbands because the lithium coin batteries can be easily accessed by children, posing a risk of serious injury or death.
KC Imports and Exports is recalling Laser & LED Light Mini Laser Pointer Keychains because button cell batteries can be easily accessed by children, posing a risk of serious injury or death.
International is recalling 2027 HV, HX, LT, MV, and RH trucks because a wiper nut may loosen, causing wipers to disconnect and reducing visibility.
Chrysler is recalling specific Mopar seat belt assemblies because the rear outboard belts may twist and fail to retract, increasing injury risk.
ResMed is recalling Astral 100/150 ventilators because supercapacitor electrolyte leakage can damage the charger chip, trigger a fail-safe state, and interrupt ventilation therapy.
Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula (Model 77522) due to potential pinhole leaks in the wire-wound body during use.
Windstone Medical Packaging is recalling 15 AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP due to supplier quality issues reported by Elevaris Medical Devices Inc.
Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula Model 77722 due to potential pinhole leaks in the wire-wound body during use.
Micro Labs USA Inc. is recalling one lot of Dorzolamide Hydrochloride and Timolol Maleate Ophthalmic Solution nationwide because the container may have broken cap spikes and undeliverable drops.
Stryker is recalling Hoffmann II Carbon Connecting Rods (catalog 50796120) because the rods may crack after cleaning and sterilization. The recall covers 5,439 units distributed worldwide.
Permobil is recalling M3 Corpus Power Wheelchairs with firmware version 1.26.2 because the firmware lacks a speed restriction when the seat lift exceeds 50 mm, which may cause falls or tip-overs.
Instrumentation Laboratory is recalling Bar Code Reader (BCR) wands used with GEM Premier 5000 and 7000 systems because they may assign patient results to the wrong patient ID.
Instrumentation Laboratory is recalling the GEM Premier 5000 portable blood analyzer system because bar code reader wands may assign patient results to the wrong patient ID. The recall affects 21 units distributed nationwide.
Mellish Island Corp. is recalling 1,600 bottles of Super Skin dietary supplement because the label does not declare that its marine collagen comes from fish, a potential allergen.
Stryker GmbH is recalling Stryker Hoffmann II Connecting Rod Micro 3 x 150mm due to the potential for the rods to crack following cleaning and sterilization processes.
Stryker GmbH is recalling Hoffmann II Carbon Connecting Rods (catalog 50796090) because they may crack after cleaning and sterilization. The FDA classified this as a Class II recall.