Blossom Pharmaceuticals recalls 15oz Zinc Oxide Ointment (NDC 75834-170-1: Lot A352318) due to cGMP deviations. Consumers should contact for details.
cGMP deviations
Blossom Pharmaceuticals is recalling a 15-ounce zinc oxide ointment product made in India due to manufacturing quality control issues. This recall does not pose an immediate safety risk to consumers but requires action to ensure product quality.
The product was manufactured in India under cGMP (current Good Manufacturing Practice) deviations, which means the production process did not meet quality standards. This could affect the product's effectiveness or safety, but it does not indicate an immediate risk of injury or illness.
Anyone who purchased the 15oz zinc oxide ointment (NDC 75834-170-15) from the manufacturer. People using the product for skin protection are most at risk due to potential quality issues.
Check for the product name 'Zinc Oxide Ointment USP, Zinc Oxide 20% Skin Protectant', 15oz (425g) size, Made in India, and lot number A352318. The NDC code is 75834-170-15.
Look for the product name, size, and lot number on the packaging to confirm if it matches the recalled item.
The recall is due to manufacturing quality control issues, not an immediate safety risk. However, consumers should follow the action steps to ensure product quality.
Check for the product name 'Zinc Oxide Ointment USP, Zinc Oxide 20% Skin Protectant', 15oz (425g) size, Made in India, and lot number A352318.
The recall does not specify a remedy, so contact Blossom Pharmaceuticals for further instructions.
We’ve drafted a message you can send Blossom Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0206-2026 — Blossom Pharmaceuticals Blossom Pharmaceuticals Hello, I own a Blossom Pharmaceuticals that is covered by recall D-0206-2026 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.
