American Regent, Inc. recalls Selenious Acid Injection, USP 12 mcg/2 mL (6 mcg/2mL), For i
See all recalls from American Regent, Inc. →Recalled Product
Selenious Acid Injection, USP 12 mcg/2 mL (6 mcg/2mL), For intravenous use, packaged in a) 2mL Single-Dose Vial (NDC 0517-6502-01), and b)10x2mL Single-Dose Vial (NDC 0517-6502-10), Rx Only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.
Hazard / Issue
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot #: 25090, Exp. Date 2/28/2027.
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Selenious Acid Injection, USP →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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