Sun Pharmaceutical recalls 150mg BuSpar tablets with dark gritty substance from desiccant canister. Customers should check bottle labels for specific lot numbers and contact the company for details.
Presence Of Foreign Substance: Customer complaint for the presence of dark, gritty substance found within the bottle which was determined to be activated carbon from the desiccant canister inside the bottle.
Sun Pharmaceutical is recalling 150mg BuSpar tablets that contain a dark, gritty substance from the desiccant canister. This could cause issues if the substance is ingested, though the risk is low and the product is not dangerous in normal use.
The tablets contain a dark, gritty substance from the desiccant canister that was accidentally included in the bottle. This could be a concern if the substance is ingested, but it is not dangerous in normal use.
People who have the 150mg BuSpar tablets with lot numbers JKX5126A, JKX5127A, JKX5128A (exp 10/2022) or similar batches. Those with the tablets in the 60-count, 100-count, or 500-count bottles are most at risk.
Check the bottle for a dark, gritty substance inside. Look for lot numbers JKX5126A, JKX5127A, JKX5128A (exp 10/2022) or similar for the 60-count bottle, and similar lot numbers for other bottle sizes.
Inspect the bottle for a dark, gritty substance that may have been accidentally included from the desiccant canister.
Reach out to Sun Pharmaceutical Industries, Inc. for specific instructions on what to do with the recalled product.
No, the dark gritty substance is not dangerous in normal use and does not pose a serious risk if the product is used as intended.
The 60-count bottle (lot numbers JKX5126A, JKX5127A, JKX5128A, exp 10/2022), 100-count bottle (JKX5126B, JKX5128B, exp 10/2022), and 500-count bottle (JKX5126C, JKX5127C, JKX5128C, exp 10/2022).
Check for the dark gritty substance and contact Sun Pharmaceutical Industries, Inc. for specific 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-0857-2022 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-0857-2022 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.
