Blossom Pharmaceuticals recalls WeCare Zinc Oxide Ointment (15 oz) due to cGMP deviations. Affected lots manufactured in India with specific expiration dates. Consumers should check labels for lot numbers and expiration dates.
cGMP deviations
Blossom Pharmaceuticals is recalling WeCare Zinc Oxide Ointment (15 oz) because of cGMP deviations. This means the product may not meet quality standards, though the recall does not specify immediate safety risks.
cGMP deviations refer to failures in manufacturing quality control processes. This could mean the ointment does not meet the required standards for purity or consistency, but the recall does not specify that it causes harm or injury.
WeCare Zinc Oxide Ointment (15 oz) users who purchased it with lot numbers A062434 (expiring June 27) or A062449 (expiring July 27) from pharmacies or retailers. People using the ointment for skin care are most at risk if they have the affected lots.
Check the product label for the lot number: A062434 (expires June 27) or A062449 (expires July 27). The ointment was manufactured in India and has a net weight of 15 oz/425 g.
Look for the lot number on the label: A062434 (expires June 27) or A062449 (expires July 27).
The recall states there were cGMP deviations, but it does not say the ointment is unsafe. Consumers should check if they have the affected lots and follow the action steps.
The recall does not specify a remedy, so the only action is to check the product label for the lot number and expiration date.
Check the label for lot numbers A062434 (expires June 27) or A062449 (expires July 27). The product was manufactured in India with a net weight of 15 oz/425 g.
We’ve drafted a message you can send Blossom Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0205-2026 — Blossom Pharmaceuticals Blossom Pharmaceuticals Hello, I own a Blossom Pharmaceuticals that is covered by recall D-0205-2026 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.
