State
73,597 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 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Hyundai is recalling 2020 Nexo and Sonata vehicles because a software defect in the Remote Smart Parking Assist system may allow unintended vehicle movement, increasing crash risk.
Forest River is recalling 2021 Starcraft Bus All Star transit buses because a wire harness may chafe against the frame, potentially causing engine stalls or loss of braking stability.
Forest River is recalling 2022 StarCraft Starquest school buses because a wire harness may chafe against the frame, potentially causing engine stalls or loss of braking stability.
Chrysler is recalling 2019-2020 RAM 2500 and 3500 trucks because the accessory bed step may fail during use, increasing injury risk.
Camso is recalling about 380 Yeti SnowMX conversion kits because the brakes can fail after installation, posing a crash hazard to users.
Pass & Seymour is recalling about 685,000 commercial-grade electrical receptacles because a manufacturing error could cause plug blades to overheat, posing a burn risk.
Yamaha is recalling 2019 XV250 motorcycles because an engine oil passageway may be blocked, causing engine stalling and increasing crash risk.
Chrysler is recalling Mopar Rear Bed Step Kits for Ram heavy-duty trucks because the bed step may fail during side loading, increasing injury risk.
Chrysler is recalling 2019-2020 Ram 1500 and Jeep Compass vehicles because windshield wiper arms may loosen, reducing visibility and increasing crash risk.
Great Dane is recalling 2020-2021 Everest Refrigerated Vans because improperly installed axle nut retaining clips may cause loose wheels and loss of vehicle control.
Marion Body Works is recalling 2019-2020 Spartan Gladiator and MetroStar vehicles because the park brake control line may loosen, potentially causing sudden deceleration and increasing crash risk.
Vac-Tron is recalling 2012-2020 vacuum excavator trailers because they may lack extended lower chassis, reducing rear impact protection and increasing crash risk.
Agility Fuel Solutions is recalling certain CNG pressure relief devices that may fail to vent when exposed to heat, potentially causing the fuel system to rupture.
New Capstone, Inc. is recalling ReStructure Vanilla Protein Powder because the ingredient statement does not include the word milk.
LeMaitre Vascular is recalling 5F Plus Over the Wire Embolectomy Catheters due to reports of deflation failure that may lead to tip separation.
Continuum is recalling Lenox 2.5 Quart Tea Kettles because they can expel hot water, posing a burn hazard. Consumers should stop using the kettles and contact the company for a refund.
Dr. Reddy's is recalling Phytonadione Injectable Emulsion ampules because they may break or shatter when opened.
Merits Health Products is recalling 82 E604 Pilot Navigator Stairlifts because the pinion gear may disengage from the track, allowing the lift to slip or jolt.
Stryker is recalling 1,415 Berchtold Chromophare Ceiling Mounted Surgical Light Systems because a missing snap ring or spanner nut may cause the light to fall.
Physio-Control is recalling 173,459 LifePAK 500 AEDs because mechanical wear on the therapy connector may prevent the device from detecting a patient, potentially delaying treatment.
Smith & Nephew is recalling 348 NAVIO Soft Tissue Protectors because the instrument may become stuck to bone pins during surgery.
Karl Storz is recalling 27,165 C-MAC Video Laryngoscopes because the glass cover at the distal end may become loose during use or reprocessing, potentially delaying procedures or requiring removal from the body.
Stryker Neurovascular is recalling AXS Vecta 71 Aspiration Catheters because they may break, fracture, or kink if improperly removed or during use.
Stryker Neurovascular is recalling 1,405 AXS Vecta 74 Aspiration Catheters because they may break, fracture, or kink if improperly removed or during use.
Bard Peripheral Vascular is recalling 150 units of the WavelinQ 4F EndoAVF System because magnetic catheters may fail to attract, potentially delaying fistula creation.