RemedyRepack Inc. recalls 300 mg Clindamycin HCl capsules due to CGMP deviations. Affected lots expire by Dec 2025. Consumers should contact the company for details.
CGMP Deviations
RemedyRepack Inc. is recalling 300 mg Clindamycin HCl capsules that were repackaged by their company. The recall is due to CGMP deviations, which means the product may not meet quality standards. This could affect safety for people using prescription antibiotics.
CGMP deviations refer to failures in manufacturing quality control processes. This could mean the capsules do not meet the required safety and purity standards for prescription medication. However, the exact risk level is not specified in the recall notice.
Prescription users of Clindamycin HCl 300 mg capsules repackaged by RemedyRepack Inc. in Indiana, PA. Those with the specific lot numbers listed in the recall are most at risk.
Check the product label for the NDC code 70518-3772-00. Look for lot numbers J0826722-121624 (expiring Dec 2025), J0820365-111324 (expiring Nov 2025), or J0814691-101624 (expiring Oct 2025).
Look for the NDC code 70518-3772-00 and specific lot numbers listed in the recall.
The recall is due to CGMP deviations, which means the product may not meet quality standards. The exact risk level is not specified in the notice.
Check the product label for the NDC code 70518-3772-00 and lot numbers J0826722-121624 (expiring Dec 2025), J0820365-111324 (expiring Nov 2025), or J0814691-101624 (expiring Oct 2025).
The recall notice does not specify a remedy or action for consumers. You should contact RemedyRepack Inc. directly for further instructions.
We’ve drafted a message you can send RemedyRepack to request your refund or repair — edit it as you like.
Subject: Recall D-0378-2025 — RemedyRepack RemedyRepack Hello, I own a RemedyRepack that is covered by recall D-0378-2025 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.
