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Class II: temporary or reversible health riskOngoing

Viona Pharmaceuticals Dapsone Gel 7 Recall

Dapsone Gel 7

VIONA PHARMACEUTICALS INC · Cranford, NJ

Risk level
Class II
Reported by FDA
Oct 23, 2024
Recall ID
D-0011-2025
Check your lot numberHow we source this data

Summary

Viona Pharmaceuticals recalled Dapsone Gel 7 starting Sep 24, 2024. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0011-2025 on Oct 23, 2024. Reason: Crystallization. Status: Ongoing.

Why it was recalled

Crystallization

Product description

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.

Lot numbers, UPCs & expiration codes

Lot #: T400512, Exp 02/28/2026

Where it was sold

NY

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0011-2025
Classification
Class II
Status
Ongoing
Recall initiated
Sep 24, 2024
FDA report date
Oct 23, 2024
Quantity
2544 pumps
Recall type
Voluntary: Firm initiated
Recalling firm
VIONA PHARMACEUTICALS INC

Original FDA data

Every field from FDA enforcement report D-0011-2025, exactly as published.

Show all FDA fields
City
Cranford
State
NJ
Status
Ongoing
Country
United States
Event ID
95412
Address
20 Commerce Dr Ste 340
Code information
Lot #: T400512, Exp 02/28/2026
Postal code
07016-3617
Report date
Oct 23, 2024
Product type
Drugs
Recall number
D-0011-2025
Classification
Class II
Recalling firm
VIONA PHARMACEUTICALS INC
Product quantity
2544 pumps
Reason for recall
Crystallization
Voluntary / mandated
Voluntary: Firm initiated
Product description
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.
Distribution pattern
NY
Recall initiation date
Sep 24, 2024
Center classification date
Oct 12, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0011-2025, published Oct 23, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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