Blossom Pharmaceuticals recalls Dynashield 4 oz cream (113g) due to cGMP deviations. Affected lots manufactured in India with specific expiration dates. Consumers should contact for details.
cGMP deviations
Blossom Pharmaceuticals is recalling Dynashield 4 oz cream (113g) because of cGMP deviations. This means the product may not meet quality standards, though the specific risk isn't detailed in the recall.
The recall is due to cGMP deviations, which are quality control issues in manufacturing. These deviations could affect the product's safety and effectiveness, but the exact risk isn't specified in the recall notice.
People who own or use Dynashield 4 oz cream (113g) with the specific lot numbers and expiration dates listed in the recall are affected. Those using the product for medical purposes may be at higher risk.
Check the product label for the lot numbers A092421 (exp. 7/27), A092340 (exp. 10/26), or A092346 (exp. 11/26). The product was manufactured in India and has the NDC code 67777-407-03.
Look for the lot numbers A092421 (exp. 7/27), A092340 (exp. 10/26), or A092346 (exp. 11/26) on the label.
The product was recalled due to cGMP deviations, which are quality control issues in manufacturing.
The recall notice does not specify a remedy, so contact Blossom Pharmaceuticals for further instructions.
The affected lots are A092421 (exp. 7/27), A092340 (exp. 10/26), and A092346 (exp. 11/26).
We’ve drafted a message you can send Blossom Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0207-2026 — Blossom Pharmaceuticals Blossom Pharmaceuticals Hello, I own a Blossom Pharmaceuticals that is covered by recall D-0207-2026 from Blossom Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.