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 expiration date on label |
| Product | 0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe. |
| Quantity | 200,000 units |
| Distribution | US Distribution in states of:OH, PA, AL, IL, TN, and CT. |
| Initiated | 2015-04-27 |
| Classified | 2015-06-04 |
| Terminated | 2016-05-02 |
| Recall number | Z-1709-2015 |
| 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-1709-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/71175/
Alerts for MRP, LLC
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.