VITRUVIAS THERAPEUTICS INC

FDA Regulatory Profile

VITRUVIAS THERAPEUTICS INC appears in FDA public data with 1 recall — including 1 Class I (most serious) —, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (D-0866-2026, Class I) was initiated on August 21, 2026.

Summary

Total Recalls
1 (1 Class I)
510(k) Clearances
0
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-0866-2026Class IThyroid Tablets, USP, 1/2 Grain (30 mg), Each tablet contains: levothyroxine (T4) 19 mcg, liothyroniAugust 21, 2026