MRP, LLC
4 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (4)
Registered facilities (1)
- Aquabiliti FEI 1000151124 · TN
Recalls & enforcement
- Class IIOngoing2023-12-28The saline flush syringes may fail to meet USP criteria for stated sodium chloride content after 12 months.
- Class IITerminated2015-07-02Procedures for the acceptance and control of in-process product have not been adequately established.
- Class IITerminated2015-04-27Incorrect expiration date on label
- Class IITerminated2015-02-09Incorrect labeling of the expiration date
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “MRP, LLC — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9076844-mrp-llc/
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