Ketorolac Tromethamine Injection, USP, 60 mg/2 mL (30 mg/mL), 2 mL Single-Dose Vial, For recall — FDA D-0036-2026
Presence of Particulate Matter: Particulate matter identified as glass
Overview of recall records associated with Aspiro Pharma Limited, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Presence of Particulate Matter: Particulate matter identified as glass
This page summarizes recall records in which the official source identifies Aspiro Pharma Limited as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.