Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the tablets.
Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the tablets.
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 Unichem Pharmaceuticals USA Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-1519-2016 — Unichem Pharmaceuticals USA Inc. Unichem Pharmaceuticals Usa Inc recalls Lamotrigine Tablets, USP, Hello, I own a Unichem Pharmaceuticals Usa Inc recalls Lamotrigine Tablets, USP, 150 mg, 500-count Tablets per bottle, Rx only, Manufactured by: Unichem Laboratories LTD., that is covered by recall D-1519-2016 from Unichem Pharmaceuticals USA 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.
