RegWardenFDA facility compliance records
Facility

Mermaid Medical A/S (FL Site)

2 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2015: 1 recalls; 2024: 1 recalls12015201620172018201920202021202220231202420252026
  • Recalls (2)

Devices registered here (1)

Recalls & enforcement

  • Class IIOngoing2024-05-01
    Internal product testing failed bubble leak testing (ASTM F2096), which indicates the sterility barrier may not be fully intact.
  • Class IITerminated2015-06-15
    Mermaid Medical A/S is recalling some of their M-Biopsy Coaxial Introducer Needles because of the potential for small plastic pieces to be present in the luer of the cannula.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Mermaid Medical A/S (FL Site) (FEI 3027260597) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3027260597-mermaid-medical-a-s-fl-site/

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