US Drug Recall Register
Class I · High risk Ongoing Initiated May 28, 2024 (2 years ago)

Docetaxel Injection, USP, 80 mg per 8 mL (10 mg per mL), 1 x 8 mL Multi-Dose Vial, Rx…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Presence of Particulate Matter: Presence of particulate matter from the stopper in the drug product.

What was recalled

Docetaxel Injection, USP, 80 mg per 8 mL (10 mg per mL), 1 x 8 mL Multi-Dose Vial, Rx only, Mfd. for Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-254-08

Recalling firm
Sagent Pharmaceuticals
NDC code
25021-254-08
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0553-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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