US Drug Recall Register
Class III · Low risk Terminated Initiated May 19, 2020 (6 years ago)

Zilretta (triamcinolone acetonide extended-release injectable suspension), 32mg per vial…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Temperature Abuse: Product was stored at room temperature longer than 6 weeks and was inadvertently distributed instead of discarded

What was recalled

Zilretta (triamcinolone acetonide extended-release injectable suspension), 32mg per vial, 5mL vials, Single-dose Kits, Rx Only, Manufactured for: Flexion Therapeutics, Inc. 10 Mall Road, Suite 301, Burlington, MA 01803, NDC 70801-003-01

Recalling firm
Flexion Therapeutics, Inc.
NDC code
70801-003-01
Origin
MA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1376-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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