State
73,092 recalls have nationwide distribution and so reach American Samoa. 25 additional recalls listed American Samoa specifically in their distribution scope.
Of the 25 recalls naming American Samoa we have scored against our rubric, 1 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 5 (20%) are Severe.
Which agencies issued them
These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Doosan is recalling 2024 Bobcat PG25 portable generator trailers because improperly tightened wheel lug nuts may allow wheels to detach, increasing crash risk.
Blue Bird is recalling 2019-2023 Vision and All American school buses because roof joints may be too weak, risking panel separation in a crash.
Ford is recalling specific front axle tie rod assemblies because incorrectly heat-treated ball studs may break, potentially causing loss of steering control.
Ford is recalling 2023-2024 Transit vehicles with the Trail package because corrosion in the steering system may cause a loss of power assist, increasing crash risk.
Hyundai is recalling 2023 Xcient vehicles because the pitman arm may not be secured properly, which can result in a loss of steering control and increase the risk of a crash.
Chrysler is recalling 2017-2018 Pacifica Plug-In Hybrid vehicles because the battery pack may cause a fire while parked. Owners should park outside and avoid charging until repairs are completed.
Chrysler is recalling 2019-2021 Pacifica Plug-In Hybrids because the battery pack may cause a vehicle fire while parked. Owners should park outside and avoid charging until repairs are completed.
CFMOTO is recalling approximately 3,630 ZFORCE 950 HO Sport Side-by-Side recreational off-highway vehicles from 2022–2023 because the shock absorber rod assembly can unthread and detach, causing suspension collapse and crash or tip-over hazards.
Honda is recalling 2024 Prologue vehicles because the right front lower control arm may contain a manufacturing defect that can fracture, causing loss of vehicle control and increasing crash risk.
Winnebago is recalling 2021–2025 Ekko motorhomes due to inadequate over-current protection in the solar charging system, which can cause the fuse to melt and increase fire risk. Dealers will replace the solar controller fuse and related components at no charge.
BISSELL is recalling about 3.2 million Steam Shot Handheld Steam Cleaners because they can expel hot water or steam during heating or use, causing burn injuries. The company has received 183 reports of hot water or steam escaping, including 157 reports of minor burn injuries.
Sassy Baby Inc. is recalling about 3,000 Manhattan Toy Brilliant Bee Rattles because the wooden base can detach and release plastic rings that pose a choking hazard to young children.
The National Highway Traffic Safety Administration is recalling certain Maserati MC20 and MC20 Cielo vehicles because their tire labels show incorrect vehicle capacity weight information, potentially causing overloading risks.
Synergetics Inc is recalling Bausch+Lomb I-PACK Intravitreal Injection Kits because sterilization certificates could not be validated by the supplier. The FDA classified this as Class I.
Suntegrity IMPECCABLE SKIN sunscreen foundation is recalled for microbial contamination with Aspergillus Sydowii mold. Consumers should discontinue use immediately.
FDA has recalled 116 units of BAUSCH+LOMB I-PACK Injection Kits because sterilization certificates could not be validated by the supplier, creating potential infection risk for patients receiving intravitreal eye injections.
Synergetics Inc is recalling the Bausch+Lomb I-PACK Injection Kit nationwide because sterilization certificates could not be validated by the supplier. The unvalidated sterilization of this eye injection device poses a potential infection risk.
Synergetics Inc is recalling 35 units of the BAUSCH+LOMB I-PACK Intravitreal Injection Kit because sterilization certificates could not be validated, creating an infection risk.
American Contract Systems Inc is recalling its ORIF HIP IM RODDING FEMUR-Procedure Kit (28 units) because ethylene oxide and ethylene chlorohydrin residuals in the cast padding exceeded safe limits for permanent implants.
American Contract Systems is recalling MAJOR KNEE surgical procedure trays due to excessive ethylene oxide and ethylene chlorohydrin residuals from sterilization that exceed safety limits for permanent exposure devices.
Cardinal Health recalls 17,445 cardiovascular procedure kits nationwide containing potentially defective syringes that could cause inaccurate dosing or device leakage.
American Contract Systems Inc is recalling 107 units of FOOT ANKLE-LF Procedure tray distributed nationwide due to ethylene oxide and ethylene chlorohydrin residuals exceeding safety limits for permanent-implant devices.
American Contract Systems is recalling a lower extremity procedure tray (48 units) due to ethylene oxide residuals that exceed FDA safety limits for permanent exposure medical devices.
Fresenius Medical Care recalls a blood pump rotor spare part used in dialysis systems in Canada due to reports of loose or dislodged guide sheaves after use. No injuries have been reported.
Fresenius is recalling blood pump rotors in home hemodialysis systems due to loose or dislodged guide sheaves reported during clinical use. The defect could affect proper pump operation during dialysis treatment.