RemedyRePack recalls 30-count Clindamycin HCl 300mg capsules (NDC 70518-3772-02) manufactured in a shared facility with Ezetimibe tablets. This recall addresses potential contamination risks from shared equipment.
CGMP Deviations - products manufactured in a shared facility with Ezetimibe tablets.
RemedyRePack is recalling 30-count Clindamycin HCl 300mg capsules (NDC 70518-3772-02) because they were made in a shared facility with Ezetimibe tablets. This could lead to contamination risks from shared equipment, though the product is prescription-only and not sold to the public.
The capsules were manufactured in a shared facility with Ezetimibe tablets, which means they could have been contaminated by equipment used for that other medication. This is a potential contamination risk, but the product is prescription-only and not sold to the public.
Prescription holders of Clindamycin HCl 300mg capsules with NDC 70518-3772-02. Patients using these capsules for medical treatment are most at risk if they have been exposed to potential contamination.
Check for the NDC number 70518-3772-02 on the bottle label. The capsules are prescription-only and sold in 30-count bottles with specific lot numbers (B3698036-033125 or B3688703-032625) expiring July 31, 2026.
Verify the NDC number 70518-3772-02 on the bottle label to confirm if your product is affected.
No, this product is prescription-only (Rx Only) and not available over the counter.
The recall does not specify a remedy, so you should check with your healthcare provider or pharmacist for guidance.
Look for the NDC number 70518-3772-02 on the bottle label, and check the lot numbers (B3698036-033125 or B3688703-032625) expiring July 31, 2026.
We’ve drafted a message you can send RemedyRePack to request your refund or repair — edit it as you like.
Subject: Recall D-0411-2025 — RemedyRePack RemedyRePack Hello, I own a RemedyRePack that is covered by recall D-0411-2025 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.
