Sun Pharmaceutical recalls 600mg Oxcarbazepine tablets with foreign substance risk. Affected lots expire 03/2023. Stop using and contact for remedy.
Presence of foreign substance
Sun Pharmaceutical is recalling 600mg Oxcarbazepine tablets that may contain a foreign substance. This could pose a health risk if taken. Affected products include 100-count, 500-count, and 1000-count bottles with specific lot numbers and expiration dates.
The tablets may contain a foreign substance that could cause harm when taken. This is a safety concern for individuals using the medication as prescribed. The exact nature of the foreign substance is not specified in the recall notice.
People who have the affected lot numbers of Oxcarbazepine tablets (100-count, 500-count, or 1000-count bottles) are likely affected. Those taking this medication for seizures or other conditions are at risk if they use the recalled products.
Check the product label for the lot numbers: HAC1474A, HAC1503A, or HAC1474B. The tablets are 600mg Oxcarbazepine, packaged in 100-count, 500-count, or 1000-count bottles with expiration dates of 03/2023.
Look for lot numbers HAC1474A, HAC1503A, or HAC1474B on the bottle.
If you have the recalled lot numbers, stop using the tablets and contact Sun Pharmaceutical for further instructions.
The recall notice does not specify what foreign substance is present.
Check the product label for lot numbers HAC1474A, HAC1503A, or HAC1474B with expiration dates of 03/2023.
Stop using the tablets immediately and contact Sun Pharmaceutical for further instructions.
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-0085-2023 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-0085-2023 from Sun Pharmaceutical. 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.
