State
73,737 recalls have nationwide distribution and so reach South Carolina. 7,152 additional recalls listed South Carolina specifically in their distribution scope.
Of the 7,152 recalls naming South Carolina we have scored against our rubric, 1,275 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,169 (30%) are Severe.
Which agencies issued them
These figures cover only the 7,152 recalls whose distribution notice names South Carolina specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
MasterPharm LLC is recalling Sildenafil 50 mg Troches nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling specific lots of Progesterone 150 mg tablets because they lack assurance of conformity to specifications.
MasterPharm LLC is recalling Yohimbine HCL 5.4mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Tadalafil 26 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Estriol 6 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
Built Brands LLC is recalling 79,500 Banana Chocolate Creme protein bars because they may be moldy before the expiration date.
MasterPharm LLC is recalling Minoxidil/Biotin/Spironolactone capsules nationwide due to a lack of processing controls and assurance of conformity to specifications.
Chengdu Ai Qin E-commerce Co., Ltd is recalling TTDEYE Flower Grey colored contact lenses because they were distributed without FDA clearance.
Allergan is recalling specific lots of Skin Medica Acne Treatment Lotion because the products failed potency tests at 12 and 24 months.
MasterPharm LLC is recalling Vardenafil 20 mg Troches nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling 462 units of Formula 82F topical solution due to a lack of processing controls that compromised product specifications.
MasterPharm LLC is recalling 543 units of Formula 82M topical solution nationwide because the product lacks assurance of conformity to specifications.
Built Brands LLC is recalling specific lots of Cookie Dough Chocolate covered protein bars because they may be moldy before the expiration date.
Steris Corporation is recalling 1,283 InnoWave Sonic Irrigators because an FDA inspection found that the foil test performed during installation lacks clear acceptance criteria.
Built Brands LLC is recalling 121,190 Black Cherry Chocolate Creme protein bars because they may be moldy before the expiration date.
MasterPharm LLC is recalling specific lots of Progesterone 150 mg Troches nationwide due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Progesterone 50 mg Modified Release Capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
Resource Optimization & Innovation LLC is recalling Regard Migrating Indicator Strips because they malfunction and fail to reach the accept window during use.
MasterPharm LLC is recalling 24 grams of Calcium citrate tetrahydrate USP powder due to a lack of processing controls that ensures conformity to specifications.
MasterPharm LLC is recalling Tadalafil 18 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
World Event Promotions, LLC is recalling Handese Advanced Instant Hand Sanitizer because the product was found to be subpotent and has high pH levels.
Sun Pharmaceutical is recalling Clonazepam Orally Disintegrating Tablets because routine stability testing detected cross-contamination with clozapine.
MasterPharm LLC is recalling Estriol 8 mg capsules nationwide due to a lack of processing controls that ensures conformity to specifications.
Smith & Nephew is recalling T-F1X0 RCG Drill Pacs because some sterile packages contain only one sleeve instead of two, preventing the device from performing as intended for the second bone tunnel.
MasterPharm LLC is recalling Finasteride Plus 1.25mg capsules nationwide because the product lacked processing controls to ensure it met specifications.