ONESOURCE SPECIALTY PHARMA LIMITED

FDA Regulatory Profile

ONESOURCE SPECIALTY PHARMA LIMITED appears in FDA public data with 1 recall, 0 510(k) clearances, 13 FDA inspections, and 1 compliance action on record. Its most recent recall (D-0662-2026, Class II) was initiated on June 7, 2026.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
13
Compliance Actions
1

Recent Recalls

NumberClassProductDate
D-0662-2026Class IIMethohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured by: OneSourcJune 7, 2026