State
72,971 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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medisca Inc. is voluntarily recalling Bimatoprost bulk powder in three sizes due to manufacturing process deviations. The powder was distributed nationwide.
Merit Medical has updated instructions for the EsophyX Z+ fastener delivery device to provide additional information about risks associated with device over-rotation and multiple fastener deployment.
Zimmer, Inc. is recalling a ceramic femoral head hip prosthesis (Model 802602203) because product labeling lacks compatibility information for use with cobalt-chrome or stainless-steel femoral stems.
Zimmer, Inc. is recalling a ceramic hip prosthesis head because the product labeling does not adequately describe compatibility with certain femoral stems used in hip replacement surgery.
Remote Diagnostic Technologies Ltd. is recalling Tempus Pro Patient Monitors due to a software issue that causes an error screen when a video laryngoscope is attached to the device.
Lupin Pharmaceuticals is recalling Clomipramine Hydrochloride Capsules (25 mg) due to an unspecified degradation product detected in stability testing. The defect was identified during an 18-month long-term stability study.
Merit Medical is updating instructions for the EsophyX Z+ Fastener Delivery Device due to risks associated with device over-rotation and multiple fastener deployment.
Zimmer, Inc. is recalling Zimmer Biomet Ceramic Head hip prostheses (Model 802802201, 22.2 mm diameter) because product labeling does not adequately provide compatibility information for use with cobalt-chrome or stainless-steel femoral stems.
OurPharma LLC is recalling HYDROmorphone Hydrochloride 50 mg/50 mL cassettes nationwide because the assay results showed higher potency than specification.
Abbott Molecular is recalling the Alinity m System due to a design flaw that may allow liquid waste or system solutions to spill beyond the instrument footprint into the user's walking path.
Straumann USA LLC is recalling 1,786 units of WB XL Anatomic Healing Abutment XC endosseous dental implant abutments due to incorrect blister labeling. The product was distributed worldwide.
Edge Biologicals is recalling Sterile Water, 3mL (Product Number T-0780, Lot 01223) due to incorrect labeling on the product's outer packaging. The affected units were distributed nationwide in Pennsylvania.
Temsa is recalling 2021-2026 TS30, TS35, and TS45 buses because a temporary bus stop valve may activate unintentionally, causing brakes to overheat and increasing fire risk.
Chrysler is recalling 2017-2019 Jeep Cherokee vehicles because a power transfer unit defect may cause loss of drive power or park function, increasing crash risk.
Dainese is recalling AGV DOT Tourmodular helmets because the chin guard plate may break, allowing the helmet to loosen or detach during a crash.
Isuzu is recalling 73 2025 NRR EV trucks because incompatible coolants may cause the cooling pump to fail, potentially leading to a loss of drive power and increased crash risk.
Key Safety Systems (Joyson) is recalling side curtain air bag inflators that may rupture due to a manufacturing defect, potentially causing injury to occupants.
Zoox is recalling 2024 robotaxis because a software defect may cause the vehicle to fail to avoid a crash when another vehicle stops perpendicularly.
Forest River Bus is recalling 453 transit buses because an incorrectly connected entry door ground wire may increase the risk of a fire.
Forest River is recalling 2025 Stealth and XLR fifth wheel travel trailers because a front exterior lamp wire lacks proper circuit protection, increasing fire risk.
Carrier is recalling specific Aspen Auxiliary Power Units because corrosion on the positive terminal block may cause a short circuit and increase the risk of a fire.
Polestar is recalling certain 2021-2025 Polestar 2 vehicles because the rearview camera image may not display when the vehicle is placed in reverse, failing FMVSS 111.
NHTSA is recalling 2025 Can-Am Origin and Pulse electric motorcycles because a faulty breather valve may allow water into the battery, risking fire or loss of power.
General Motors is recalling certain 2021-2024 Escalade, Silverado 1500, Suburban, Tahoe, Sierra 1500, Yukon and Yukon XL vehicles with 6.2L V8 engines because connecting rod or crankshaft defects can cause engine failure.
AliExpress-sold RGB LED strip lights are recalled because children can easily access the coin batteries inside, creating a serious ingestion hazard. Swallowed batteries can cause severe internal burns and death.