EPI Health recalls minolira (minocycline hydrochloride) 105mg extended-release tablets with potential quality control issues. Affected lots manufactured by Dr Reddy's Laboratories in India. Consumers should contact the manufacturer for details.
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 (minocycline hydrochloride) 105mg extended-release tablets because the manufacturer discontinued their quality control program. This could mean the product doesn't meet safety standards, but the recall doesn't specify immediate risks to users.
The manufacturer discontinued their quality control program, which could mean the product doesn't meet the required safety and purity standards. This might affect the medication's effectiveness or safety, but the recall doesn't specify how this impacts users.
People who have been prescribed minolira 105mg extended-release tablets by a doctor. Those with specific medical conditions requiring this medication may be at higher risk if the product is unsafe.
Check for the product name 'minolira' (minocycline hydrochloride) 105mg extended-release tablets, 30-count bottle. Look for lot numbers T2300765, T2201702A, T2201699, or T2201698 with expiration dates up to February 2025.
Identify the lot number and expiration date on the packaging to determine if it's affected.
The recall states there was a quality control issue, but it does not specify if the product is unsafe. Consumers should contact the manufacturer for details.
The recall does not provide specific action steps. Contact EPI Health directly for guidance.
Check the lot number on the packaging. Affected lots include T2300765, T2201702A, T2201699, and T2201698 with expiration dates up to February 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-0474-2024 — EPI Health EPI Health Hello, I own a EPI Health that is covered by recall D-0474-2024 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.
