Alembic Pharmaceuticals recalls 200mg Celecoxib capsules due to customer complaints finding Tadalafil 5mg tablets inside sealed bottles. Affected units contain batch 2405014780, expiring Sep 2027.
Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil 5mg tablet inside a sealed 500-count bottle of Celecoxib 200mg capsule
Alembic Pharmaceuticals is recalling 200mg Celecoxib capsules because customers found Tadalafil 5mg tablets inside sealed bottles. This could cause unintended medication intake if taken without knowing.
The recall is triggered by customer complaints finding Tadalafil 5mg tablets inside sealed bottles of Celecoxib 200mg capsules. This means users might accidentally take the Tadalafil tablets if they don't notice the foreign tablets in their bottle.
Prescription users of Celecoxib 200mg capsules in the US who received the specific batch (2405014780) from Alembic Pharmaceuticals. People with arthritis or other conditions requiring this medication are most at risk.
Check for Celecoxib 200mg capsules in 500-count bottles with NDC 62332-142-71, batch 2405014780, expiring September 2027. The product is only available through prescription.
Look for Tadalafil 5mg tablets inside the sealed Celecoxib 200mg capsule bottle.
Customer complaints found Tadalafil 5mg tablets inside sealed bottles of Celecoxib 200mg capsules.
Check your bottle for Tadalafil 5mg tablets. If found, stop using the product and contact your doctor.
The product is safe if you don't find Tadalafil 5mg tablets inside the bottle. Otherwise, it could cause unintended medication intake.
We’ve drafted a message you can send Alembic to request your refund or repair — edit it as you like.
Subject: Recall D-0459-2025 — Alembic Alembic Hello, I own a Alembic that is covered by recall D-0459-2025 from Alembic. 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.
