Golden State Medical Supply recalls 150mg Rifampin Capsules due to impurities exceeding safety limits. This could cause serious injury if taken. Check NDC numbers and lot dates for affected batches.
Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).
Golden State Medical Supply is recalling 150mg Rifampin Capsules because they contain impurities above safe levels. Taking these capsules could cause serious injury. Affected products have specific NDC and lot numbers listed in the recall.
The capsules contain impurities that exceed the 5 ppm safety limit for 1-Methyl-4-Nitrosopoperazine (MNP). This chemical can cause serious injury if taken as directed. The impurities are a result of failed quality control during manufacturing.
Prescription patients who have the recalled Rifampin Capsules. Those with the specific NDC numbers and lot dates listed in the recall are most at risk.
Check for the NDC number 51407-322-30 on the bottle. Look for lot numbers GS036715 through GS046111 with expiration dates listed in the recall. The product is prescription-only and sold under the brand name Rifampin Capsules.
Immediately stop using the recalled Rifampin Capsules if you have them. Do not take any more capsules from this batch.
The capsules contain 1-Methyl-4-Nitrosopoperazine (MNP) at levels exceeding the 5 ppm safety limit.
Check the NDC number 51407-322-30 on the bottle and look for lot numbers listed in the recall (GS036715 through GS046111).
The recall record does not mention any replacement or refund options.
We’ve drafted a message you can send Golden State Medical Supply to request your refund or repair — edit it as you like.
Subject: Recall D-0012-2023 — Golden State Medical Supply Golden State Medical Supply Hello, I own a Golden State Medical Supply that is covered by recall D-0012-2023 from Golden State Medical Supply. 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.
