MRP, LLC dba AMUSA
MRP, LLC dba AMUSA has 3 FDA enforcement events on this register (3 product records) between 2015 and 2015: 3 device; the busiest year was 2015 with 3.
0% of its events are Class I; the most common class is Class II (3). 0 events are listed as ongoing; the recalling firm's address is in TN.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 2 Jul 2015 | 0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution. | Device | Class II | 1 | Terminated |
| 27 Apr 2015 | 0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe. | Device | Class II | 1 | Terminated |
| 9 Feb 2015 | 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. | Device | Class II | 1 | Terminated |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has MRP, LLC dba AMUSA had?
3 enforcement events (3 product records) on this register, 2015–2015: 3 device.
Are any MRP, LLC dba AMUSA recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are MRP, LLC dba AMUSA recalls?
3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.