Failed USP Dissolution Test Requirements: The recalled lots do not meet the specification for dissolution.
Failed USP Dissolution Test Requirements: The recalled lots do not meet the specification for dissolution.
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 Prometheus Laboratories Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-1659-2012 — Prometheus Laboratories Inc. Prometheus Laboratories Inc. recalls Mercaptopurine Tablets, USP, 50 m Hello, I own a Prometheus Laboratories Inc. recalls Mercaptopurine Tablets, USP, 50 mg, packaged in a) 60-count tablets per bottle (NDC 49884-922-02) and b) 250-count that is covered by recall D-1659-2012 from Prometheus Laboratories Inc.. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
