FDA Drugs recall ·
Dapsone Gel 7.5%, 60 gram pump, Rx Only, Manufactured by: Zydus… recall
- Recall number
- D-0038-2025
- Date
- (initiated October 29, 2024)
- Company / brand
- Viona Pharmaceuticals Inc
20 Commerce Dr Ste 340, Cranford, NJ, United States - Category
- Drugs › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 6048 pumps
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Dapsone Gel 7.5%, 60 gram pump, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Viona Pharmaceuticals Inc., Cranford, NJ 07016, NDC 72578-094-02.
Why was it recalled?
Crystallization
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
Lots T401151, Exp, 06/30/2026; T400806, Exp 03/31/2026
Distribution
USA Nationwide
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (drugs), recall D-0038-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.