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Medium risk Drugs & MedicationsClass II

Baxter Healthcare Corporation Recall

Clindamycin Injection USP in 5% Dextrose, 900 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Single Dose Container, Rx only, Sterile Nonpyrogenic

Updated August 6, 2026

Baxter Healthcare Corporation is recalling Clindamycin Injection USP in 5% Dextrose, 900 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Single Dose Container, Rx only, Sterile Nonpyrogenic. Hazard: CGMP Deviations

Is the Baxter Healthcare Corporation recalled? Yes. This product was recalled by FDA on August 6, 2026. Details below.

What is recalled

Clindamycin Injection USP in 5% Dextrose, 900 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-3814-50.

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

CGMP Deviations

Brands affected

Baxter Healthcare Corporation
Source
FDA
Category
Drugs & Medications
Recall ID
fda-D-0815-2026
Classification
Class II
Recalled
August 6, 2026
Read the official notice

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