State
73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2014-2017 F-150 trucks with 3.5L engines because the brake master cylinder may leak fluid, increasing the risk of a crash.
Forest River is recalling 2021 Prime Time Avenger travel trailers because safety chains may be incorrectly attached, posing a risk of total trailer separation.
Maxon Lift Corp. is recalling specific lift gates where the license plate light may aim rearward, failing federal safety standards and increasing crash risk.
Mercedes-Benz is recalling 2020 GLE 450, GLS 450, and GLS 580 4MATIC vehicles because leaking suspension components may affect handling and increase crash risk.
Mercedes-Benz is recalling 2020 E450, GLC300, and AMG models because the left-rear seatback latch may fail, increasing injury risk in a crash.
Jayco is recalling certain 2019–2021 Class C motorhomes because the Operator's Manual contains incorrect information about the automatic parking function, which could lead to unintended vehicle movement or rollaway.
Braun Ambulances is recalling 31 Demers ambulances because a rear brake line may wear, causing brake failure and increasing crash risk.
General Motors is recalling 2020 Chevrolet Silverado and GMC Sierra trucks because improperly heat-treated hood-latch striker wires may fracture, allowing the hood to open while driving.
Jaguar Land Rover is recalling 2016 Range Rover and Range Rover Sport vehicles because a previous repair may have failed, allowing the left door to remain unlatched.
Capstone Holdings is recalling Simply Earth Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.
Honda is recalling 2019 Clarity Fuel Cell, Electric, and Plug-in Hybrid vehicles because the rear seat belt locking mechanism may not function as intended, increasing injury risk in a crash.
Tim Trading is recalling Emori Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.
Quest Medical is recalling MPS Top Cover Replacement Kits because additive and arrest agent labels were swapped, posing a risk of over-delivering potassium during surgery.
Biomet is recalling 15 units of Regenerex Series-A Patella knee prostheses due to potential endotoxin levels exceeding specifications.
Siemens is recalling 20 Cios Spin X-Ray systems because unplugging the monitor cable can create unsafe voltage, posing an electrical shock hazard.
Biomet, Inc. is recalling 46 units of Vanguard Knee System tibial bearings because they may contain elevated endotoxin levels that exceed specification limits.
Philips is recalling 21,683 sets of sterilizable defibrillator internal paddles because they may wear over time and fail to deliver therapy if routine checks are not performed.
Nikon Metrology is recalling 110 XTH cabinet x-ray systems because interior shielding may detach, potentially causing x-ray emissions to exceed safety limits.
Intuitive Surgical is recalling 305 da Vinci SP cameras because residual soil on the tip may affect image quality or cause patient sensitization.
Philips is recalling 260 HeartStart MRx Monitor/Defibrillators because some units may not have received required corrections from prior field actions.
Biomet, Inc. is recalling 105 units of Vanguard M Partial Knee System MonoBlock Tibial Trays due to potential elevated endotoxin levels.
Biomet is recalling 93 Vanguard Knee System tibial bearings due to potential endotoxin levels exceeding specifications. The recall covers units distributed worldwide.
Philips is recalling 130 HeartStart XL Monitor/Defibrillators because they may not have received required corrections from prior field actions.
Biomet, Inc. is recalling specific RingLoc Hip System components due to potential elevated endotoxin levels that exceed specification limits.
Spectranetics is recalling Bridge Occlusion Balloons because current labeling is insufficient to warn users about the risk of thrombus formation if the device remains in the vasculature for long durations.