Class II — MRP, LLC dba AMUSA
| Recalling firm | MRP, LLC |
|---|---|
| Registered facility | Aquabiliti (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Procedures for the acceptance and control of in-process product have not been adequately established. |
| Product | 0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution. |
| Quantity | 551 cases |
| Distribution | Distributed in the states of CA. PA, VA, TX, MA, MD, WV, UT, FL, and TN. |
| Initiated | 2015-07-02 |
| Classified | 2015-08-27 |
| Terminated | 2017-04-03 |
| Recall number | Z-2476-2015 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — MRP, LLC dba AMUSA (Z-2476-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/71735/
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