MXBBB recalls 850mg hyaluronic acid capsules due to possible contamination with undeclared diclofenac and omeprazole. No confirmed analytical data exists for the affected lots.
cGMP Deviations: the firm initiated a recall after notification from the distributor that product may be tainted with undeclared diclofenac and omeprazole, however there is no analytical data confirming that product distributed by the firm is tainted.
MXBBB is recalling 850mg hyaluronic acid capsules that may contain undeclared diclofenac and omeprazole. This recall is based on distributor notifications, but no confirmed analytical data shows the product is tainted.
The recall was initiated after a distributor reported potential contamination with undeclared diclofenac and omeprazole. However, the manufacturer states there is no analytical data confirming the product is actually tainted.
People who own or use the recalled 850mg hyaluronic acid capsules with UPC 7502265120323 are affected. Those with the specific lot number 24183 are at higher risk.
Check for the UPC 7502265120323 on the product label. The affected lot number is 24183, with an expiration date of July 1, 2028.
Look for the UPC 7502265120323 and lot number 24183 on the capsule packaging.
The manufacturer states there is no confirmed analytical data showing the product is tainted with diclofenac or omeprazole, so it may be safe.
MXBBB initiated the recall after a distributor reported potential contamination with undeclared diclofenac and omeprazole.
The recall record does not mention any remedy or corrective action for this product.
We’ve drafted a message you can send MXBBB to request your refund or repair — edit it as you like.
Subject: Recall D-0166-2025 — MXBBB MXBBB Hello, I own a MXBBB that is covered by recall D-0166-2025 from MXBBB. 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.
