Busulfan Injection, 60 mg per 10 mL (6 mg per mL), 8x10 mL Single-Dose Vials, Rx only, Mfd. for Sagent Pharmaceuticals,
Sagent Pharmaceuticals
Failed Impurities/Degradation Specifications
1 recall found for Sagent Pharmaceuticals — May 2026.
The recalls listed below are active notices associated with Sagent Pharmaceuticals in the FDA, NHTSA, USDA, and CPSC databases. None of the current recalls are classified as urgent. Check the specific lot numbers, model numbers, or production date codes in each notice carefully — a recall typically covers specific production runs, not everything a manufacturer sells.
A manufacturer appearing in the recall database does not indicate an ongoing safety failure. High-volume companies with large product lines naturally appear more frequently. What matters is whether your specific product — identified by lot number, model number, or date code — is included in a recall notice.
Browse all medication recalls →Sagent Pharmaceuticals
Failed Impurities/Degradation Specifications