Blossom Pharmaceuticals recalls Lanashield Skin Barrier 4 oz. products due to cGMP deviations. Affected lots have specific expiration dates and manufacturing details. Consumers should check their product labels for the lot numbers and expiration dates listed.
cGMP deviations
Blossom Pharmaceuticals is recalling Lanashield Skin Barrier 4 oz. products made for Dynarex Corporation due to cGMP deviations. This means the products may not meet quality standards and could pose a risk to consumers.
cGMP deviations refer to failures in the manufacturing process that could affect product quality and safety. These deviations might result in the product not meeting the required standards for skin barrier protection.
People who own or use Lanashield Skin Barrier 4 oz. products with the specific lot numbers and expiration dates listed in the recall notice are affected. Those using the product for sensitive skin or frequent application may be at higher risk.
Check the product label for the lot number and expiration date. The affected products have lot numbers A162301 (exp. 9/26), A162401 (exp. 4/27), and A162202 (exp. 11/25).
Look for the lot number and expiration date on the product label to determine if it is affected.
Blossom Pharmaceuticals is recalling Lanashield Skin Barrier due to cGMP deviations, which are manufacturing process failures that could affect product quality and safety.
The affected lot numbers are A162301 (exp. 9/26), A162401 (exp. 4/27), and A162202 (exp. 11/25).
The recall does not specify a stop-use instruction, so you can continue using the product if it is not affected.
We’ve drafted a message you can send Blossom Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0201-2026 — Blossom Pharmaceuticals Blossom Pharmaceuticals Hello, I own a Blossom Pharmaceuticals that is covered by recall D-0201-2026 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.
