Aspiro Pharma Limited

FDA Regulatory Profile

Aspiro Pharma Limited appears in FDA public data with 1 recall, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (D-0036-2026, Class II) was initiated on October 1, 2025.

Summary

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

Recent Recalls

NumberClassProductDate
D-0036-2026Class IIKetorolac Tromethamine Injection, USP, 60 mg/2 mL (30 mg/mL), 2 mL Single-Dose Vial, For IntramusculOctober 1, 2025