Rising Pharma is recalling 1000-count Pregabalin 50mg capsules due to foreign tablets found during packaging. This is a safety issue for prescription users.
Presence of Foreign Tablets/Capsules: Complaint received from a re-packager, American Health Packaging (AHP), where a foreign tablet was discovered in one of the bottles during packaging set up. Tablet identified as pantoprazole tablet 20mg.
Rising Pharma is recalling 1000-count Pregabalin 50mg capsules because foreign tablets (pantoprazole) were found in some bottles during packaging. This could pose a risk if someone takes the wrong medication.
Foreign pantoprazole tablets (a different medication) were found in some bottles of Pregabalin capsules during packaging. If someone takes the foreign tablets instead of the intended medication, they could get an incorrect dose or side effects.
Prescription users of Pregabalin 50mg capsules who received this specific bottle from Rising Pharma. People taking the medication for nerve pain or seizures are most at risk if they accidentally take the foreign tablets.
Check for the bottle labeled 'Pregabalin Capsules 50mg, 1000-count' with NDC 64980-411-10. The lot number is 23132611, expiring 07/31/2026. This product was manufactured by Laurus Labs Limited in India.
Look for foreign tablets (pantoprazole) in the bottle before taking any doses.
No, the recall is only for the foreign tablets found during packaging. If you take the correct Pregabalin capsules, it is safe.
Check for the bottle labeled 'Pregabalin Capsules 50mg, 1000-count' with NDC 64980-411-10 and lot number 23132611.
No, you can continue using the product as long as you check for foreign tablets before taking doses.
We’ve drafted a message you can send Rising Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0541-2024 — Rising Pharma Rising Pharma Hello, I own a Rising Pharma that is covered by recall D-0541-2024 from Rising Pharma. 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.
