State
73,827 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 9 (36%) are Severe.
Which agencies issued them
These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Prevost is recalling 2015-2016 X3-45 buses because cracks in sliding passenger seats may compromise structural integrity, increasing injury risk in crashes.
Spartan Motors is recalling 2016-2017 SB school bus chassis because a parking brake cable clip may fail, causing the vehicle to roll unexpectedly.
Prevost is recalling specific 2011-2016 coach models because a missing clip allows the coolant line to rub against the fuel hose, potentially causing a fuel leak and engine compartment fire.
Hardkore Karts is recalling 2009-2013 Club Car Precedent golf carts with street packages that lack required VINs, certification labels, and DOT-compliant windshields.
Nova Bus is recalling 863 LFS and LFS Artic buses from 2014-2016 because a wiper idler arm pin may strip, causing wipers to stop working and reducing visibility.
Universal Trailer is recalling 2007-2010 Haulmark Motorcoaches because a bolt may fracture, causing entry steps to become unstable and increasing injury risk.
Strick is recalling certain single axle van trailers because rear impact guard gussets increase injury risk in crashes.
Toyota is recalling specific 2008-2010 Lexus SC, Corolla, Corolla Matrix, and Pontiac Vibe vehicles because the front passenger air bag inflator may rupture during deployment.
KME is recalling 2015-2016 Predator emergency vehicles because the gearbox may shift to neutral while driving, increasing crash risk.
Pelican Products is recalling specific 9410L flashlights and replacement battery packs because the lithium-ion batteries can overheat and cause fires. No injuries have been reported.
Cook Inc. is recalling 1,341 single-lumen central venous catheter sets and trays due to a manufacturing defect that may cause catheter tip fracture or separation.
Xeridiem is recalling 326 EndoVive 3s Low Profile Balloon Kits because the feeding valve may close inconsistently, allowing fluid to leak.
Cook Inc. is recalling 9,519 Shuttle Select Slip-Cath Catheters worldwide due to reports of catheter tip splits and separation, which can cause loss of function or complications.
Draeger Medical is recalling Evita Infinity V500 and Babylog Infinity VN500 ventilators because the optional PS500 power supply unit batteries may discharge prematurely despite showing adequate charge.
Xeridiem is recalling 189 EndoVive 3s Low Profile Balloon Kits because the feeding valve may close inconsistently, allowing fluid to leak.
Cook Inc. is recalling 2,280 single-lumen pressure monitoring sets and trays because a manufacturing defect may cause catheter tips to fracture or separate.
Cook Inc. is recalling radial artery pressure monitoring catheter sets because a manufacturing defect may cause the catheter tip to fracture or separate.
Bergstrom is recalling ParkSmart HVAC units for Freightliner Cascadia trucks due to a connector defect that may cause overheating and increase the risk of a fire.
Xeridiem Mediem Medical Devices Inc is recalling 36 EndoVive 3s Low Profile Balloon Kits because the feeding valve may close inconsistently, allowing fluid to leak.
Xeridiem is recalling 126 EndoVive 3s Low Profile Balloon Kits because the feeding valve may close inconsistently, allowing fluid to leak.
Xeridiem Mediem Medical Devices Inc is recalling 39 EndoVive 3s Low Profile Balloon Kits because the feeding valve may close inconsistently, allowing fluid to leak.
Cook Inc. is recalling specific femoral artery pressure monitoring catheter sets and trays because a manufacturing defect may cause the catheter tip to fracture or separate.
Xeridiem is recalling 34 EndoVive 3s Low Profile Balloon Kits because the feeding valve may leak gastric contents when disconnected.
Forest River is recalling 176 recreational vehicles due to an ignition switch defect that may cause stalling or loss of safety systems.
Maquet is recalling seven Flow-i Anesthesia Systems in the US due to electrical issues in control and monitoring sub-systems that can cause restarts or system disabling.