Sun Pharmaceutical recalls 300mg gabapentin capsules (NDC 62756-138-04/05) due to cross contamination risk. Affected lots expire 2025. Consumers should contact Sun Pharmaceutical for details.
Cross Contamination
Sun Pharmaceutical is recalling 300mg gabapentin capsules that may have cross contamination. This recall affects specific packaging lots that expire in 2025. The cross contamination risk means the medication might not be safe for patients with certain conditions.
Cross contamination occurs when the capsules are produced in a facility that also handles other medications, potentially introducing harmful substances. This could affect patients with specific health conditions that require strict medication purity.
People who have the specific 500-count or 1000-count bottles of gabapentin capsules with the listed NDC numbers and expiration dates. Patients with conditions requiring precise medication dosing are most at risk.
Check for 500-count bottles (NDC 62756-138-05) or 1000-count bottles (NDC 62756-138-04) with expiration dates of 04/2025 or 07/2025 or 08/2025.
Look for the NDC numbers 62756-138-04 or 62756-138-05 on the bottle and expiration dates matching the listed dates.
Sun Pharmaceutical recalls these gabapentin capsules due to cross contamination risk.
The capsules may have been contaminated with other medications during production, potentially affecting patients with specific health conditions.
Check for 500-count bottles (NDC 62756-138-05) or 1000-count bottles (NDC 62756-138-04) with expiration dates of 04/2025, 07/2025, or 08/2025.
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-0311-2025 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-0311-2025 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.
