Recalls / Brands / Carboplatin
Carboplatin
4 FDA drug recalls involving brand “Carboplatin” — 2 Class I.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2012-11-08 | Class I | Carboplatin Injection, 450 mg/45 mL (10 mg/mL), 45 mL, Cytotoxic Agent, Sterile, Multi-Dose Vial, Rx only, For | Hospira Inc. |
| 2012-11-08 | Class I | Carboplatin Injection, 600 mg/60 mL (10 mg/mL), 60 mL, Cytotoxic Agent, Sterile, Multi-Dose Vial, Rx only, For | Hospira Inc. |
| 2012-07-02 | Class III | Carboplatin Injection, 10 mg/mL, a) 5 mL multi-dose vials (NDC 61703-339-18) (NDC 61703-360-18, NOVAPLUS), b) | Hospira Inc. |
| 2012-06-27 | Class II | Carboplatin Injection, 10 mg/mL, 45 mL Multi-Dose Vial, Rx only, antineoplastic/cytotoxic agent; Manufactured | Hospira Inc. |