Micro Labs Limited recalls 10mg Clobazam tablets due to residual solvents outside specifications. This may pose health risks. Contact for return instructions.
CGMP Deviations: Out of specification for residual solvents.
Micro Labs Limited is recalling 10mg Clobazam tablets because they contain unsafe levels of residual solvents. This could lead to health issues if taken as directed.
The tablets were made with residual solvents that don't meet safety standards. This could cause health problems if taken as prescribed, though the exact risk level isn't specified.
People with prescriptions for Clobazam tablets from Micro Labs Limited in the U.S. are affected. Those with the specific 100-count bottle are most at risk.
Check for the 100-count bottle labeled 'Clobazam Tablets 10mg, Rx Only' with NDC code 42571-315-01. The product was manufactured by Micro Labs Limited in India and distributed by Micro Labs USA, Inc. in the U.S.
Look for the NDC code 42571-315-01 on the bottle label to confirm it's the recalled item.
The tablets were made with residual solvents that don't meet safety standards.
Check for the 100-count bottle labeled 'Clobazam Tablets 10mg, Rx Only' with NDC code 42571-315-01.
The recall record does not specify a remedy or action steps.
We’ve drafted a message you can send Micro Labs to request your refund or repair — edit it as you like.
Subject: Recall D-0348-2024 — Micro Labs Micro Labs Hello, I own a Micro Labs that is covered by recall D-0348-2024 from Micro Labs. 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.
