Recall Ledger

Busulfan Injection recall (Sagent Pharmaceuticals)

DrugClass IIIOngoing

Summary: Sagent Pharmaceuticals is recalling Busulfan Injection, 60 mg per 10 mL (6 mg per mL), 8x10 mL Single-Dose Vials, Rx only, Mfd. for Sagent Pharmaceuticals, Schaumburg, IL 60195, Made in Canada, NDC 25021-241-10.. Reason: Failed Impurities/Degradation Specifications.

What is being recalled

Busulfan Injection, 60 mg per 10 mL (6 mg per mL), 8x10 mL Single-Dose Vials, Rx only, Mfd. for Sagent Pharmaceuticals, Schaumburg, IL 60195, Made in Canada, NDC 25021-241-10.

Why

Failed Impurities/Degradation Specifications

How serious is it

Class III is the least serious level: using or being exposed to this product is not likely to cause health problems, but it breaks FDA rules.

Where it was sold

Nationwide within the United States

How to tell if yours is affected

Lot #: 656412, Exp. Date 08/31/2026; 659646, Exp. Date 03/31/2027.

What to do

Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.

Recall facts

Recall numberD-0539-2026
CategoryDrug
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass III
StatusOngoing
Recall startedMay 4, 2026
ReportedMay 27, 2026
CompanySagent Pharmaceuticals
Company locationSchaumburg, IL, United States
Initiated byVoluntary: Firm initiated
QuantityLot 656412: 6,200 vials. Lot 659646: 3,328 vials.

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