State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kia is recalling 2014-2016 Soul and Soul EV vehicles because a pinion plug defect may allow the pinion gear to separate, potentially causing loss of steering and increasing crash risk.
Mitsubishi is recalling 2015-2017 Outlander, Outlander Sport, Lancer, and Lancer Evolution vehicles because defective relays may cause engine stalls, reduced power, or overheating.
Maserati is recalling 2015-2017 Quattroporte GTS vehicles because a fuel pump resistor may fail, causing engine stall and increasing crash risk.
Hino is recalling 3,224 trucks because worn engine parts may cause failure, increasing crash risk.
BMW is recalling 2006-2010 X3 vehicles because the front passenger seat occupant detection mat may crack, potentially deactivating the air bag in a crash.
Silver Eagle is recalling 2018 Vast-20W converter dolly trailers because brake caliper bolts may not be properly torqued, risking caliper detachment and loss of braking ability.
Skip Hop is recalling about 130,000 Moonlight & Melodies nightlight soothers because the USB wall power adapter can break, posing an electrical shock hazard.
Wabash is recalling 2012-2013 converter dolly trailers because fasteners may loosen, allowing the counterweight tube to detach while in motion, increasing crash risk.
America New York RI Wang Food Group is recalling approximately 63,823 pounds of pork and beef sausage products due to misbranding and an undeclared milk allergen.
Pfizer is recalling specific lots of Levophed (norepinephrine bitartrate) injection because a damaged sterilizing filter may have compromised sterility.
Pfizer is recalling 115,370 vials of Hydromorphone Hydrochloride Injection because a damaged sterilizing filter may have compromised sterility assurance during manufacturing.
Genentech is recalling 16,882 units of Activase (alteplase) because the included sterile water vials may have cracked or chipped glass.
Polar Tank is recalling 2018 SRJ7 trailers because brake caliper bolts may not be properly torqued, risking caliper detachment and loss of braking ability.
Amgen is recalling specific lots of Procrit (epoetin alfa) vials because glass flakes were found during routine quality inspection.
NOW Foods is recalling Organic Coconut Sugar because it contains undeclared gluten despite being labeled 'Gluten Free'.
DICK's Sporting Goods is recalling about 207,500 Fitness Gear resistance tubes because they can break and strike users. Consumers should stop using them and return them for a refund or store credit.
YSN Imports is recalling Flame King RV outdoor cooktop stoves because an internal cover can burn if the flame inverts, increasing the risk of a fire.
Bearing Technologies is recalling Duralast Wheel Spindles for 2007-2010 Ford Edge vehicles because oversized studs may prevent correct wheel installation, increasing crash risk.
Medtronic is recalling Solarice Rapid Exchange Balloon Dilatation Catheters due to stylette removal difficulties. The recall covers 105,633 units distributed worldwide.
Medisca, Inc. is recalling Aminocaproic Acid API lots because the product was manufactured for industrial use but labeled for pharmacy compounding.
PharMEDium Services is recalling 295 bags of compounded Fentanyl Citrate because the diluent used was expired before the product's assigned expiration date.
Beckman Coulter is recalling AQUIOS CL Flow Cytometer systems because a software configuration error may cause the device to draw samples from the wrong tube, resulting in incorrect laboratory values.
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because they no longer meet release liner removal specifications.
Medtronic is recalling Euphora Rapid Exchange Balloon Dilatation Catheters due to stylette removal difficulties. The recall covers 69,081 units distributed in the US and worldwide.
PharMEDium Services is recalling 590 bags of compounded Fentanyl Citrate because the diluent used was expired before the product's assigned expiration date.