Drug recall
0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution.
FDA recall event 71735 · Class II · MRP, LLC dba AMUSA
Key facts
| Event ID | 71735 |
|---|---|
| Recall numbers | Z-2476-2015 |
| Recalling firm | MRP, LLC dba AMUSA |
| Product type | Devices |
| Products | 0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Procedures for the acceptance and control of in-process product have not been adequately established. |
| Initiation date | Jul 2, 2015 |
| Report date | Sep 2, 2015 |
| Termination date | Apr 3, 2017 |
| City | Nashville |
| State | TN |
| Country | United States |
| FEI number | 1000151124 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: