Blossom Pharmaceuticals recalls Wecare Enema due to cGMP deviations. Affected lots manufactured in India with specific expiration dates. Consumers should check their product details to determine if recalled.
cGMP deviations
Blossom Pharmaceuticals is recalling Wecare Enema products made in India due to cGMP deviations. This means the products may not meet quality standards, though the exact risk is not specified in the recall notice.
cGMP deviations refer to failures in manufacturing quality control processes. This could mean the product does not meet safety and quality standards, but the recall does not specify the exact risk or how it might affect users.
Anyone who owns or uses the Wecare Enema product with the described lot numbers and expiration dates. People using the product for medical purposes are most at risk.
Check the product label for the lot numbers A022310 (exp. 2/26), A022335 (exp. 10/26), A022406 (exp. 12/27), or A022505 (exp. 12/27). The product was manufactured in India and sold with NDC 67777-402-01.
Look for the lot numbers A022310, A022335, A022406, or A022505 on the product label.
The recall states there were cGMP deviations, but does not specify if the product is unsafe. Consumers should check if their product has the listed lot numbers.
The recall does not provide a remedy, so there is no action required beyond checking if your product has the listed lot numbers.
Check the product label for the lot numbers A022310, A022335, A022406, or A022505 with the specified expiration dates.
We’ve drafted a message you can send Blossom Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0203-2026 — Blossom Pharmaceuticals Blossom Pharmaceuticals Hello, I own a Blossom Pharmaceuticals that is covered by recall D-0203-2026 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.
