CGMP Deviations
CGMP Deviations
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 SUN PHARMACEUTICAL INDUSTRIES INC to request your refund or repair — edit it as you like.
Subject: Recall D-0869-2023 — SUN PHARMACEUTICAL INDUSTRIES INC SUN PHARMACEUTICAL INDUSTRIES INC recalls Buprenorphine Sublingua Hello, I own a SUN PHARMACEUTICAL INDUSTRIES INC recalls Buprenorphine Sublingual Tablets, 8 mg, 30 count-bottles, Rx only, Manufactured by: Sun Pharma, NDC 62756-460-83. that is covered by recall D-0869-2023 from SUN PHARMACEUTICAL INDUSTRIES 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.
