US Drug Recall Register
Class I · High risk Ongoing Initiated Dec 23, 2024 (2 years ago)

Prograf (tacrolimus) capsules, USP, 0.5 mg, 100-count bottle, Rx Only, Product of Japan…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain empty capsules

What was recalled

Prograf (tacrolimus) capsules, USP, 0.5 mg, 100-count bottle, Rx Only, Product of Japan, Distributed by: Astellas Pharma US, Inc., Northbrook, IL 60062, NDC 0469-0607-73.

Recalling firm
Astellas Pharma US Inc.
NDC code
0469-0607-73
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0211-2025

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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