Preferred Pharmaceuticals is recalling 300mg Clindamycin Hydrochloride Capsules (30-count) manufactured by Glenmark Pharmaceuticals due to cGMP deviations. This may affect safety.
cGMP Deviations
Preferred Pharmaceuticals is recalling 300mg Clindamycin Hydrochloride Capsules (30-count bottles) made by Glenmark Pharmaceuticals because of manufacturing deviations. This recall is due to potential quality issues that could affect safety.
The recall is due to cGMP deviations, which are manufacturing quality issues. These deviations could potentially affect the safety and effectiveness of the medication. However, the specific risk to users is not clearly described in the recall notice.
People who own or use the recalled Clindamycin Hydrochloride Capsules (300mg, 30-count) manufactured by Glenmark Pharmaceuticals are affected. Those taking this medication for medical treatment are most at risk.
Check for Clindamycin Hydrochloride Capsules, USP, 300mg, 30-count bottles with NDC 68788-8685-03. The lot numbers L0224T, K1824M, K0124N, J1624V, J0824O, I2424E, I1024O, A0925F, L2324L and expiration date 7/31/2026 are also indicators.
Look for the NDC code 68788-8685-03 and lot numbers listed in the recall notice.
The recall mentions cGMP deviations but does not specify if the medication is dangerous. The official notice does not describe the specific risk to users.
Check for Clindamycin Hydrochloride Capsules, USP, 300mg, 30-count bottles with NDC 68788-8685-03 and lot numbers L0224T, K1824M, K0124N, J1624V, J0824O, I2424E, I1024O, A0925F, L2324L, expiring 7/31/2026.
The recall does not specify a remedy, so the official notice does not state what action to take.
We’ve drafted a message you can send Preferred Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0391-2025 — Preferred Pharmaceuticals Preferred Pharmaceuticals Hello, I own a Preferred Pharmaceuticals that is covered by recall D-0391-2025 from Preferred Pharmaceuticals. 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.
