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 | Incorrect labeling of the expiration date |
| Product | T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL Single Use Syringe, Rx only, Part no. 2S0706 Usage: Flush syringe. |
| Quantity | 1,080 units (3 cases) |
| Distribution | US distribution to CA only. |
| Initiated | 2015-02-09 |
| Classified | 2015-06-15 |
| Terminated | 2015-06-22 |
| Recall number | Z-1808-2015 |
| 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-1808-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/70974/
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