Eugia US LLC (f/k/a Auro Medics Pharma LLC) Issues Voluntary Nationwide Recall of Vancomycin Hydrochloride for Injection USP 1.25g/Vial-30mL (Single Dose Vial) Due to Presence of Particulate Matter
- Date
- Nov 6, 2026
- Company
- Eugia US LLC
- Brand
- Eugia
- Product
- Vancomycin Hydrochloride for Injection USP 1.25g/Vial-30mL (Single Dose Vial)
- Reason
- Presence of particulate matter identified as a glass particle inside the vial
- Hazard
- Other
- Source
- FDA
How to identify the product
- November 06,2026 – East Windsor, New Jersey, Eugia US LLC (f/k/a Auro Medics Pharma LLC) is voluntarily recalling lot number 3VM26026A of Vancomycin Hydrochloride for Injection USP 1.25g/Vial-30mL (Single Dose Vial) to the hospital/healthcare facility/user level due to the presence of particulate matter identified as a glass particle inside the vial.
- The recalled product is packaged in 30 mL vial and packed as 10 (vials) X 10 (Printed cartons) X 01 (Shipper) with NDC code as 55150-471-01.
- The product can be identified by product name on carton (NDC 55150-471-10) and vial (NDC 55150-471-01) label and with lot number 3VM26026A and Exp.
- Eugia US LLC shipped the entire lot to wholesalers nationwide from September 2, 2026, through September 15, 2026.
- The Company is notifying its distributors and customers by recall letters and is arranging for return/replacement of all recalled products.
- Wholesalers/hospitals/pharmacies, institutions, and doctors with existing inventory of the recalled product lot should discontinue use and quarantine the product immediately.
Where to find the lot number or date code on your package →
Product photos are on the official FDA page.
Facts are taken from the official notice. If anything here differs from it, the official notice is correct.