FDA Drug Recalls

Recalls / Class II

Class IID-0207-2026

Product

Dynashield, 4 oz cream (113 g), Manufactured for: Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10852, USA, Made in India, NDC 67777-407-03.

Brand name
Dynashield
Generic name
Zinc Oxide
Active ingredient
Zinc Oxide
Route
Topical
NDC
67777-407
FDA application
M016
Affected lot / code info
Lot #: A092421, Exp. Date 7/27, A092340, Exp. Date 10/26 & A092346, Exp. Date 11/26.

Why it was recalled

cGMP deviations

Recalling firm

Firm
Blossom Pharmaceuticals
Manufacturer
Dynarex Corporation
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
Plot No. 21/22 Bardez Blossom Pharmaceuticals Karaswada-Tivim, Bardej, Goa, N/A, India

Distribution

Quantity
7944 containers
Distribution pattern
USA Nationwide

Timeline

Recall initiated
2025-10-31
FDA classified
2025-12-02
Posted by FDA
2025-12-10
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0207-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.