State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
STIHL is recalling about 73,000 PolyCut mowing heads because loose bolts can cause the unit to come apart, posing an injury risk.
Walker Edison Furniture is recalling about 1,200 children's bunk beds because support boards can break, posing fall and injury hazards.
Pfizer is recalling specific lots of Relpax (eletriptan HBr) tablets because they may be contaminated with Burkholderia and Pseudomonas bacteria.
Siemens is recalling 17 Artis zee and Artis Q interventional X-ray systems because cracks in the patient table mainframe could cause the upper bed to detach, posing a hazard to patients and staff.
Siemens is recalling SOMATOM go.Top CT scanners because the injector holder could fall off with the injector and storage box.
Siemens is recalling three SOMATOM go.Up CT systems because the injector holder could fall off with the injector and storage box.
Kawasaki is recalling about 2,600 Teryx and Teryx4 recreational off-highway vehicles because an incorrect joint assembly can cause loss of steering control, posing crash and injury hazards.
Stryker GmbH is recalling 76 units of the Endintrak 2 Hook Blade because the sterile bag seal may be compromised, potentially affecting sterility.
Abbott is recalling Alinity ci series System Control Modules because a software issue may cause incorrect test results after a system stop.
Siemens Medical Solutions is recalling SOMATOM go.All CT scanners because the injector holder could fall off with the injector and storage box.
Artizen Oils is recalling wintergreen and birch essential oils because the bottles lack required child-resistant caps, posing a poisoning risk to young children.
John Deere is recalling about 19,730 XUV835 Gator utility vehicles because the throttle cable sheathing can melt, causing the throttle to stick and posing a crash hazard.
Siemens is recalling SOMATOM go.Now CT systems because the injector holder could fall off with the injector and storage box.
Siemens is recalling 12 SOMATOM go.Top CT scanners because the injector holder could fall off. The devices are distributed in 20 US states.
Stryker GmbH is recalling 21 Endotrac EPF/EGR Triangle Blades because the sterile bag seal integrity may be compromised, posing a risk of contamination.
Stryker GmbH is recalling 476 Endotrac ECTR Push Blades because the sterile bag seal integrity may be compromised, potentially affecting sterility.
CooperSurgical is recalling TransWarmer Warming Infant Transport Mattresses because some units lack updated instructions prohibiting use with other heat devices, which could cause skin burns.
Siemens is recalling 10 SOMATOM go.All CT scanners because the injector holder could fall off. The units are distributed in 20 US states.
John Deere is recalling Frontier grooming mowers because incorrect driveline assembly can prevent the safety shield from spinning, posing an entanglement injury risk.
Siemens is recalling 18 SOMATOM go.Up CT systems because the injector holder could fall off, posing a risk of injury.
Stryker GmbH is recalling 110 units of Endotrac EPF/EGR Hook Blades because the sterile bag seal integrity may be compromised.
Stryker GmbH is recalling 53 Endotrac ECTR Triangle Blades because the sterile bag seal may be compromised, potentially affecting sterility.
Stryker GmbH is recalling 259 Endintrak 2 Hook Blade kits because the sterile bag seal integrity may be compromised, potentially affecting sterility.
Stryker GmbH is recalling 1,959 Endotrac ECTR Hook Blades because the sterile bag seal may be compromised, potentially affecting sterility.
Ad-Tech Medical Instrument Corporation is recalling Skull Anchor Bolts because supplemental information incorrectly indicated they were approved for use in the MR environment.