FDA Recall D-0202-2026

Blossom Pharmaceuticals

Class II Ongoing 195 days on record

Moderate impact — Class II recall — temporary or medically reversible adverse health consequence possible; remote probability of serious adverse health consequence.

Product

Dynashield Skin Protectant, Net Wt. 16 oz (453.6 g), Manufactured for: Dyrnarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962, USA, Made in India, NDC 67777-407-04.

Lot / code: Lot #: A092334, Exp. Date 6/26 & A092421, Exp. Date 7/27

Quantity: 1560 containers

Reason for recall

cGMP deviations

Recall record

Recall number: D-0202-2026
Classification: Class II
Status: Ongoing
Voluntary or mandated: Voluntary: Firm initiated
Firm notification: Letter
Distribution: USA Nationwide
Recall initiated: 2025-10-31
Classified by FDA Center: 2025-12-02
FDA published: 2025-12-10
Recalling firm: Blossom Pharmaceuticals

Drug identification

Brand name(s): DYNASHIELD
Generic name(s): ZINC OXIDE
Manufacturer(s): Dynarex Corporation
NDC(s): 67777-407
Route(s): TOPICAL

Operational response

Class II recalls indicate possible temporary or reversible health consequences. Remove affected lots from active dispensing. Segregate inventory. Check the firm’s recall notification for guidance on patient outreach.

For the official FDA enforcement record, see FDA's Recall Search.

‹ All recalls