MRP, LLC dba Aquabiliti

FDA Regulatory Profile

MRP, LLC dba Aquabiliti appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1174-2024, Class II) was initiated on December 28, 2023.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1174-2024Class IIAQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe, USP, 5mL in 12mL, REF 2T0805; and 3mL inDecember 28, 2023