Drug recall D-0293-2015
Product
Famotidine Injection 20 mg, Rx Only, GALAXY Single Dose Container, Code 2G3424, Sterile Nonpyrogenic, 50 mL Iso-osmotic, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-5197-41.
Reason for recall
Presence of Particulate Matter: Baxter Healthcare Corporation has received a complaint reporting the presence of particulate matter identified as plastic/rubber in famotidine Injection premixed containers.
Lots and codes
Lot #: NC082768, Exp 12/23/2014
Recall details
- Recalling firm
- Baxter Healthcare Corp., Deerfield, IL
- Quantity
- 19,152 Containers
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- April 24, 2014
- Terminated
- June 16, 2015
Related products
- Famotidine – drug information
- NDC 0338-5197 Famotidine · Famotidine 20 mg/50mL · Baxter Healthcare Corporation