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.
Mercedes-Benz is recalling 2018-2019 C300 and C43 AMG vehicles because the 12-volt battery bracket may be unsecured, risking terminal disconnection in a crash.
Mercedes-Benz is recalling one 2019 S 450 vehicle because improperly installed pillar covers may prevent side curtain air bags from deploying correctly during a crash.
Dennis Eagle is recalling one 2017 Diego vehicle because a switch failure may cause instrument controls to move sides and disable the electronic braking system.
Forest River is recalling 2020 Columbus Fifthwheel Trailers because the rear ladder blocks the egress window, preventing emergency exit.
Navistar is recalling 2,677 IC school buses because the roof hatch external handle may break, preventing emergency egress.
Navistar is recalling 2019-2020 IC RE and IC CE commercial buses because the roof hatch external handle may break, potentially preventing emergency egress.
ImprimisRx NJ is recalling 246 bottles of Timolol-Dorzolamide-Latanoprost ophthalmic drops because the medication was found to be subpotent.
Qiagen Sciences LLC is recalling specific lots of Filter-Tips used with QIAsymphony instruments because a small percentage of tips are leaking.
LNK International is recalling specific lots of Equate Nighttime Sleep Aid because of microbial contamination in the non-sterile product.
Jubilant Cadista Pharmaceuticals is recalling specific lots of Drospirenone and Ethinyl Estradiol Tablets because they failed dissolution specifications during stability testing.
Burlington Medical is recalling 49 radiation protection caps because the protective material may not adequately shield users from scatter radiation.
Siemens Healthcare Diagnostics Inc is recalling Stratus CS Acute Care cTNI TestPaks due to a potential for increased false positive results.
Burlington Medical is recalling Porta Shield radiation protection products because the material may provide inadequate protection against scatter radiation.
Burlington Medical is recalling 129 two-piece radiation protection vests and kilts because the protective material may provide inadequate shielding against scatter radiation.
Burlington Medical is recalling two half aprons because the protective material may provide inadequate protection against scatter radiation, potentially exposing users to higher radiation levels.
Burlington Medical is recalling 807 thyroid collars because the protective material may provide inadequate protection against scatter radiation, potentially increasing long-term health risks.
Burlington Medical is recalling three radiation protection hoods because the protective material may not adequately shield users from scatter radiation.
Burlington Medical is recalling Frontal Aprons with Quick Drop Velcro Closure because the protective material may provide inadequate protection against scatter radiation.
Burlington Medical is recalling two radiation protection aprons because the protective material may provide inadequate shielding, potentially exposing users to scatter radiation.
Burlington Medical is recalling 39 radiation protection sleeves because the material may provide inadequate protection against scatter radiation.
Burlington Medical is recalling seven Overlap Vests because the protective material may provide inadequate protection against scatter radiation.
Burlington Medical is recalling 332 lead apron products because the protective material may provide inadequate protection against scatter radiation.
Burlington Medical is recalling nine Frontal Stretch Buckle Closure Aprons because the protective material may provide inadequate protection against scatter radiation.
Burlington Medical is recalling six Frontal Support Belt Aprons because the protective material may provide inadequate protection against scatter radiation.
GE Healthcare is recalling 82 Senographe Pristina mammography systems because the biopsy positioner may slip when the gantry is rotated during a procedure.