Blossom Pharmaceuticals recalls Dynagel Moisturizing Wound Hydrogel due to cGMP deviations. Affected lots expire 7/26 and 8/26. Consumers should check product labels for lot numbers.
cGMP deviations
Blossom Pharmaceuticals is recalling Dynagel Moisturizing Wound Hydrogel products made for Dynarex Corporation. The recall is due to cGMP deviations, which means the product may not meet quality standards.
cGMP deviations refer to failures in the manufacturing process that could affect product quality. This means the hydrogel might not be safe or effective for wound care, potentially causing infection or delayed healing.
People who own or use Dynagel Moisturizing Wound Hydrogel products with lot numbers A322301 (expiring 7/26) or A322302 (expiring 8/26) are affected. Those with open wounds or using the product for medical purposes are at higher risk.
Check the product label for lot numbers A322301 (expiring 7/26) or A322302 (expiring 8/26). The product is a 3oz (84.7 g) Moisturizing Wound Hydrogel manufactured by Dynarex Corporation.
Look for lot numbers A322301 (expiring 7/26) or A322302 (expiring 8/26) on the label.
The recall is due to cGMP deviations, which means the product may not meet quality standards. It is not safe to use as intended.
Check the product label for lot numbers A322301 (expiring 7/26) or A322302 (expiring 8/26). If you have these lots, contact Blossom Pharmaceuticals for instructions.
The recall record does not specify a replacement option. Consumers should contact Blossom Pharmaceuticals for further assistance.
We’ve drafted a message you can send Blossom Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0204-2026 — Blossom Pharmaceuticals Blossom Pharmaceuticals Hello, I own a Blossom Pharmaceuticals that is covered by recall D-0204-2026 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.
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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.
