Class II
Terminated
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.
This recall has been terminated (originally issued December 17, 2014).
- Company
- Baxter Healthcare Corp.
- Recall Initiated
- April 24, 2014
- Posted
- December 17, 2014
- Recall Number
- D-0293-2015
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 19,152 Containers
- Firm Location
- Deerfield, IL, United States
- Official Source
- View on FDA website ↗
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.
Distribution
Nationwide
Lot / Code Info
Lot #: NC082768, Exp 12/23/2014
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