Failed Dissolution Specifications: Product found to be out of specification (OOS) during stability testing.
Failed Dissolution Specifications: Product found to be out of specification (OOS) during stability testing.
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-0249-2015 — Prometheus Laboratories Inc. Prometheus Laboratories Inc. recalls Mercaptopurine Tablets, USP 50mg, Hello, I own a Prometheus Laboratories Inc. recalls Mercaptopurine Tablets, USP 50mg, a) 60-count bottle (NDC 49884-922-02), b) 250-count bottle (NDC 49884-922-04), RX that is covered by recall D-0249-2015 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.
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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.
