FDA Drugs recall ·
Triamcinolone Acetonide Cream USP, 0.025%, 1 LB (454 g) per jar, Rx Only… recall
- Recall number
- D-0048-2025
- Date
- (initiated October 11, 2024)
- Company / brand
- Padagis US LLC
3940 Quebec Ave N, Minneapolis, MN, United States - Category
- Drugs › Class III
- Classification
- Class III
- Status
- Terminated
- Units affected
- 10,872 jars
- Hazard tags
- Potency
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Triamcinolone Acetonide Cream USP, 0.025%, 1 LB (454 g) per jar, Rx Only, Manufactured By Padagis, Minneapolis, MN 55427. NDC: 45802-0063-05
Why was it recalled?
Subpotent and Superpotent Drug. Out of specification assay results recorded as part of Uniformity of Container test during long-term stability testing.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot #: 2024154238, 2024174344, Exp. Date 3/31/2026
Distribution
Nationwide in the USA
What does Class III mean?
Class III means use of or exposure to the product is not likely to cause adverse health consequences (for example, a labeling violation).
Source: FDA (drugs), recall D-0048-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.