RemedyRepack Inc. recalls 300 mg Rifampin Capsules due to failed impurities and degradation specifications. This Rx-only medication may pose risks if not used properly.
Failed Impurities/Degradation specifications
RemedyRepack Inc. is recalling 300 mg Rifampin Capsules (30-count blister packs) because they failed impurities and degradation tests. This could lead to unsafe drug levels if taken as prescribed.
The capsules failed impurities and degradation specifications, meaning they might not contain the correct drug levels. This could cause treatment failure or side effects if taken as directed.
Prescription patients who received these specific Rifampin Capsules from RemedyRepack Inc. are affected. Patients on long-term antibiotic treatment are most at risk due to potential medication inefficacy.
Check for the 300 mg Rifampin Capsules in 30-count blister packs with the Repackaged NDC 70518-2404-00. The lot numbers J0599794-022322 (exp. 02/28/2023) and J0621369-052622 (exp. 06/30/2023) are also identifiers.
Verify the product label for the Repackaged NDC 70518-2404-00 and lot numbers J0599794-022322 or J0621369-052622.
The capsules failed impurities and degradation specifications, which could lead to incorrect drug levels and treatment failure.
Check the product label for the Repackaged NDC 70518-2404-00 and lot numbers to confirm if it's affected. No specific action is required beyond verification.
This recall is for medication efficacy, not immediate safety risks. The hazard is low risk as it relates to treatment effectiveness, not physical harm.
We’ve drafted a message you can send RemedyRepack to request your refund or repair — edit it as you like.
Subject: Recall D-0098-2023 — RemedyRepack RemedyRepack Hello, I own a RemedyRepack that is covered by recall D-0098-2023 from RemedyRepack. 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.
