FDA Device recall Z-2476-2015
0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution
- FDA Device
- Class II
- terminated
- Published 2015-09-02
On 2015-09-02 the FDA classified a Class II recall of 0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution by Mrp, citing procedures for the acceptance and control of in-process product have not been adequately established.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2476-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-02 |
| Published | 2015-09-02 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Mrp |
| Distribution | CA, FL, MA, MD, PA, TN, TX, UT, VA, WV |
Product
0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution.
Reason
Procedures for the acceptance and control of in-process product have not been adequately established.
Identifiers
| code_info | KH04143,exp. 07/2016; KH04145, exp. 08/2016; KH04153, exp. 11/2016; KH04155, exp. 12/2016 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2476-2015%22
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