State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Infiniti Creations, LLC is voluntarily recalling Slim Life HCG Drops due to misbranding and potential undeclared HCG content.
Synthes (USA) Products LLC is recalling 114 sterile extraction hooks because their peel pouches are delaminating, potentially compromising sterility.
Infiniti Creations, LLC is voluntarily recalling Health & Beyond 2oz HCG Drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling HCG Diet Plan drops due to misbranding and potential undeclared HCG content.
Synthes (USA) Products LLC is recalling 887 sterile 3.0 mm reaming rods because their peel pouches are delaminating.
Synthes (USA) Products LLC is recalling 198 units of Flexible Shaft orthopedic surgical instruments because non-conforming material was used in their manufacture.
Infiniti Creations, LLC is voluntarily recalling Natural Protocols 2oz HCG Drops due to misbranding and potential undeclared HCG content.
Synthes (USA) Products LLC is recalling 260 sterile 2.5 mm TI Calibrated Reaming Rods because their peel pouches are delaminating.
West-Ward Pharmaceuticals is recalling specific lots of Phenobarbital Tablets because they failed to meet dissolution specifications at the 12-month stability time point.
Infiniti Creations, LLC is voluntarily recalling HCG ASAP drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling Simeons Program HCG Drops due to misbranding and potential undeclared HCG content.
Pentax of America is recalling video colonoscopes shipped between April 2014 and September 2015 because they included outdated instruction manuals and lacked required reprocessing adaptors.
Infiniti Creations is voluntarily recalling HCG Drops due to misbranding and potential undeclared HCG content.
Merit Medical Systems is voluntarily recalling 107,341 Fluid Administration Sets due to a molding defect in the drip chamber.
Synthes (USA) Products LLC is recalling 319 sterile 3.0 mm Guide Rods because their peel pouches are delaminating.
Zydus Pharmaceuticals USA Inc. is recalling BUPROPION Hydrochloride Extended-Release Tablets, 300 mg, because the product failed to meet dissolution specifications at an intermediate time point.
Infiniti Creations, LLC is voluntarily recalling A New You HCG Drops due to misbranding and potential undeclared HCG content.
Synthes (USA) Products LLC is recalling 139 units of 2.5 mm Guide Rods because their sterile peel pouches are delaminating.
Infiniti Creations, LLC is voluntarily recalling SkinEHCG HCG Drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling Original HCG Drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling HCG Plus drops due to misbranding and potential undeclared HCG content.
Sun Pharmaceutical Industries is recalling KENALOG (Triamcinolone Acetonide) Spray due to low alcohol content. The product failed stability specifications.
Synthes (USA) Products LLC is recalling 1,951 sterile 2.5 mm reaming rods because their peel pouches are delaminating.
Mylan Pharmaceuticals is recalling Diltiazem HCl Extended-Release Capsules because of out-of-specification results for a known compound.
Synthes (USA) Products LLC is recalling 5,478 sterile 3.0 mm reaming rods because their peel pouches are delaminating.