FDAFDA · Food and drugs·Recall number Z-2476-2015
0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution.
Published September 2, 2015 · Recall initiated: July 2, 2015
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Procedures for the acceptance and control of in-process product have not been adequately established.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- MRP, LLC dba AMUSA
- Distributor
- Distributed in the states of CA. PA, VA, TX, MA, MD, WV, UT, FL, and TN.
- Lot
- KH04143,exp. 07/2016; KH04145, exp. 08/2016; KH04153, exp. 11/2016; KH04155, exp. 12/2016
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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