EPI Health is recalling minolira (minocycline hydrochloride) 135mg extended-release tablets, 30-count bottles manufactured by Dr Reddy's. The recall is due to a quality control deviation that may affect product safety.
CGMP Deviation: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess.
EPI Health is recalling minolira 135mg extended-release tablets because of a quality control issue at the manufacturer. This could mean the medication doesn't meet safety standards, so it's important to check if you have the recalled product.
The manufacturer discontinued their quality control program, which means the product might not meet the required safety and purity standards. This could lead to the medication not working as intended or causing health issues.
People with prescriptions for minolira 135mg extended-release tablets from EPI Health. Those who have the specific lot numbers or expiration dates listed in the recall are most at risk.
Check for the product name 'minolira' (minocycline hydrochloride) 135mg extended-release tablets, 30-count bottle. Look for lot numbers T2201700 or T2201701 with an expiration date of 02/28/2025.
Look for the product name, lot numbers T2201700 or T2201701, and expiration date 02/28/2025 on the packaging.
The manufacturer discontinued their quality control program, which could mean the product doesn't meet safety and purity standards.
The recall record does not specify a remedy, so check with your healthcare provider or the manufacturer for guidance.
Check for the product name 'minolira' (minocycline hydrochloride) 135mg extended-release tablets, 30-count bottle with lot numbers T2201700 or T2201701 and expiration date 02/28/2025.
We’ve drafted a message you can send EPI Health to request your refund or repair — edit it as you like.
Subject: Recall D-0475-2024 — EPI Health EPI Health Hello, I own a EPI Health that is covered by recall D-0475-2024 from EPI Health. 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.
