Eugia US LLC 2023-01-11 Health serious FDA
Health · FDA · Recall #FDA-D-0095-2023
Acyclovir Sodium Injection 1,000 mg per 20 mL* (50 mg/mL); Single Dose 20mL Vial, Rx… Recall
Issued January 11, 2023 · Eugia US LLC
In January 2023, Eugia US LLC recalled the Acyclovir Sodium Injection 1,000 mg per 20 mL* (50 mg/mL); Single Dose 20mL Vial, Rx…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Presence of Particulate Matter: Customer complaint of dark particles found inside the vial
What you should do
- 1 Stop using Acyclovir Sodium Injection 1,000 mg per 20 mL* (50 mg/mL); Single Dose 20mL Vial, Rx… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Eugia US LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Eugia US LLC
- Category
- Health
- Recall date
- January 11, 2023
- Units affected
- Not reported
- Sold at
- Nationwide in the USA
- Recall number
- FDA-D-0095-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Eugia US LLC has 13 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.