Sagent Pharmaceuticals: Famotidine Injection, 200 Mg Per
- Recalling firm
- Sagent Pharmaceuticals
- Product
- Famotidine Injection, 200 mg per 50 mL (4 mg per mL), 1 x 50 mL Multi-Dose Vial, For Intravenous Use, Rx only, Sterile, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60173. NDC: 25021-756-50
- Reason
- Presence of Particulate Matter
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-10-22
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/c64ff943-11ca-4f0a-8e37-a08c184226d8