Sun Pharmaceutical recalls 500-count and 1000-count Gabapentin 400mg capsules due to cross contamination risk. Affected lots expire March 2025. Consumers should check NDC codes and lot numbers.
Cross Contamination
Sun Pharmaceutical is recalling certain Gabapentin 400mg capsules that may have cross contamination. This could lead to unintended medication interactions if the capsules are taken without proper cleaning. The recall affects specific lot numbers and packaging sizes.
Cross contamination means the capsules could have been exposed to other substances during manufacturing, potentially causing unintended medication interactions. This risk is low but requires careful handling to avoid adverse effects.
Prescription patients who received the recalled 500-count or 1000-count bottles of Gabapentin 400mg capsules with specific NDC numbers and lot numbers. People taking this medication for conditions like neuropathic pain or seizures are most at risk.
Check for 500-count bottles with NDC 62756-139-05 or 1000-count bottles with NDC 62756-139-04. The lot numbers are HAD1712B (expiring March 2025) or HAD1712C (expiring March 2025).
Identify the NDC code (62756-139-05 for 500-count bottles or 62756-139-04 for 1000-count bottles) and lot number (HAD1712B or HAD1712C) on the packaging.
Cross contamination means the capsules may have been exposed to other substances during manufacturing, potentially causing unintended medication interactions.
Check for 500-count bottles with NDC 62756-139-05 or 1000-count bottles with NDC 62756-139-04, and lot numbers HAD1712B or HAD1712C.
No, the recall does not require stopping use immediately. However, you should check the product details to confirm if it is recalled.
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-0312-2025 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-0312-2025 from Sun Pharmaceutical. 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.
