Eugia US LLC recalls Acyclovir Sodium Injection vials due to customer reports of dark particles. This may cause injury if injected. Check your vial's lot number and contact the manufacturer for details.
Presence of Particulate Matter: Customer complaint of dark particles found inside the vial
Eugia US LLC is recalling Acyclovir Sodium Injection vials after customers reported dark particles inside the vials. This could cause injury if the particles are injected into the body.
Dark particles found in the vials could potentially cause injury if injected into the body. The hazard is reported through customer complaints, not through testing or known manufacturing defects.
People who have been prescribed Acyclovir Sodium Injection by a doctor. Those using the product for medical treatment are most at risk.
Check for vials labeled 'Acyclovir Sodium Injection 1,000 mg per 20 mL (50 mg/mL), Single Dose 20mL'. Look for lot number AC22004 with expiry date 08/2023.
Look for the lot number AC22004 and expiry date 08/2023 on the vial label.
The recall is due to customer reports of dark particles, but the product is not safe to use as it may cause injury if injected.
Check for vials labeled 'Acyclovir Sodium Injection 1,000 mg per 20 mL (50 mg/mL), Single Dose 20mL' with lot number AC22004 and expiry date 08/2023.
The recall does not specify a remedy, so contact the manufacturer for further instructions.
We’ve drafted a message you can send Eugia to request your refund or repair — edit it as you like.
Subject: Recall D-0095-2023 — Eugia Eugia Hello, I own a Eugia that is covered by recall D-0095-2023 from Eugia. 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.
