US Drug Recall Register
Class I · High risk Completed Initiated Nov 8, 2012 (14 years ago)

Carboplatin Injection, 450 mg/45 mL (10 mg/mL), 45 mL, Cytotoxic Agent, Sterile…

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

Why it was recalled

Crystallization: Product is being recalled due to visible particulates identified during a retain sample inspection. Findings have identified the particles as Carboplatin crystals.

What was recalled

Carboplatin Injection, 450 mg/45 mL (10 mg/mL), 45 mL, Cytotoxic Agent, Sterile, Multi-Dose Vial, Rx only, For IV Use, NDC 61703-339-50 (Hospira label) and NDC 61703-360-50 (Novaplus label), Hospira, Inc., Lake Forest, IL 60045, Product of Australia.

Recalling firm
Hospira Inc.
NDC code
61703-339-50
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-154-2013

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.

Other Carboplatin recalls

See all