CGMP Deviations: These products are being recalled because they were manufactured with active pharmaceutical ingredients (APIs) that were not manufactured with good manufacturing practices.
CGMP Deviations: These products are being recalled because they were manufactured with active pharmaceutical ingredients (APIs) that were not manufactured with good manufacturing practices.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Caraco Pharmaceutical Laboratories, Ltd. to request your refund or repair — edit it as you like.
Subject: Recall D-1511-2014 — Caraco Pharmaceutical Laboratories, Ltd. Caraco Pharmaceutical Laboratories, Ltd. recalls Cephalexi Hello, I own a Caraco Pharmaceutical Laboratories, Ltd. recalls Cephalexin Capsules, USP, 500 mg, packaged in a) 100-count bottles (NDC 62756-294-88) and b) 500-count bottles (NDC that is covered by recall D-1511-2014 from Caraco Pharmaceutical Laboratories, Ltd.. 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.
