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Drug FDA Class II Ongoing cGMP deviation

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

Blossom Pharmaceuticals Published Dec 10, 2025

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 60/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Blossom Pharmaceuticals or your place of purchase with questions, and see the source record below for full details.
Reason for recall

cGMP deviations

Affected products (1)

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

DYNASHIELD · 7944 containers

NDC: 67777-407, 67777-407-01, 67777-407-02, 67777-407-03, 67777-407-10, 67777-407-04, 67777-407-11, 67777-407-12, 67777-407-13
Code info: Lot #: A092421, Exp. Date 7/27, A092340, Exp. Date 10/26 & A092346, Exp. Date 11/26.

Affected areas

Nationwide

Timeline

  1. Initiated
    Oct 31, 2025
  2. Published
    Dec 10, 2025
Recall number
D-0207-2026
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA drug enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.