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.
ARBOC is recalling 2017-2026 Spirit of Independence transit buses because incorrect washers on rear spring hanger bolts may cause the hanger to detach, increasing crash risk.
Mercedes-Benz USA, LLC is recalling certain 2020-2026 Mercedes-Benz vehicles because a faulty door lock micro-switch may cause the vehicle to roll away.
Frontrunner is recalling 2025 transit buses because wheelchair retractors may fail to lock, increasing injury risk. Owners will be notified to have parts replaced.
EnHomee 9-Drawer Fabric Dressers sold on Walmart.com pose a risk of serious injury or death from tip-over and entrapment if not anchored to the wall. About 16,809 units are affected.
BMW is recalling certain 2020-2026 S 1000 RR motorcycles because vibration may cause ignition lock failure, leading to engine stalls or electrical system failures.
About 670 Sviyatp pool drain covers sold online violate federal safety standards and pose entrapment and drowning hazards. Consumers should stop using affected pools immediately and contact Sviyatp for a refund.
Romorgniz 12-Drawer Fabric Dressers sold on Amazon pose tip-over and entrapment risks to children if not anchored to the wall. About 10,040 units are affected.
K&N Engineering is recalling specific K&N and Spectre replacement fuel filters because the O-ring may disintegrate, causing leaks or clogs.
CuddleCubs Creations Baby Highchair Teething Toy Sets are recalled due to pull-string teething toys that violate mandatory toy safety standards. The silicone strings can lodge in a child's throat, creating a risk of choking and respiratory distress.
OeyUoc white pool drain covers sold on Amazon violate safety standards and pose entrapment and drowning risks. About 404 units have been recalled; consumers should stop using them immediately.
Forest River is recalling 2026-2027 Pause and OG Luxury Coach RVs because a rooftop fan circuit board may overheat and cause a fire.
Aojieni Silicone is recalling about 5,918 Sili Factory Pull String Teething Toys because the silicone strings violate toy safety standards and can lodge in a child's throat, posing a serious choking risk.
Peony Design has recalled personalized baby bibs and stroller bags sold online because snaps can detach, posing a choking risk to young children. The company is offering refunds.
Forest River is recalling 2027 travel trailers because the Federal Placard may list an incorrect fresh water tank capacity, which could lead to vehicle overloading.
Argon Medical Devices is recalling General Biopsy Tray kits containing Lidocaine HCL Injection because the kits do not meet sterility release criteria.
Abiomed is recalling ABIOMED Insertion Kits due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines. The manufacturing defect is not visually detectable by users.
Abiomed is recalling the Impella RP Flex heart pump due to potential introducer sheath leakage from the sheath cap and hub score lines. The manufacturing defect is not visually detectable.
Argon Medical Devices is recalling One-Piece Introducer Tray kits containing Lidocaine HCL Injection because they do not meet sterility release criteria. The kits were distributed nationwide and internationally.
Argon Medical Devices is recalling T-Lok Bone Marrow Tray kits containing Lidocaine HCL Injection USP 1% because the kits did not meet sterility release criteria.
Abiomed is recalling the Impella CP Smart Assist Set due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines in 14Fr and 23Fr introducers. These manufacturing issues are not visually detectable.
Argon Medical Devices is recalling an Arterial Line Kit containing Lidocaine HCL Injection USP because the kits do not meet sterility release criteria, creating a risk of infection from non-sterile medical injection.
ABIOMED is recalling Impella CP heart pump sets worldwide due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines in 14Fr and 23Fr introducers. The manufacturing defect is not visually detectable.
Abiomed is recalling Impella 5.5 SmartAssist S2 heart pump sets worldwide due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines that may not be visible to users.
ICU Medical is recalling the Plum Solo Precision IV Pump (v1.0.3) because in specific scenarios, the pump may fail to decrease the displayed volume and could deliver up to twice the programmed medication amount.
ABIOMED Impella CP heart pump sets contain introducers that may leak from under the sheath cap and along hub score lines. These manufacturing defects are not visible during use.