Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Docetaxel Injection Recalled by Sagent Pharmaceuticals Due to Presence of Particulate Matter: Presence of particulate matter...

Date: May 28, 2024
Company: Sagent Pharmaceuticals
Status: Ongoing
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Sagent Pharmaceuticals directly.

Affected Products

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

Quantity: 762 vials

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Sagent Pharmaceuticals

Sagent Pharmaceuticals has 6 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report