RegWardenFDA facility compliance records
Facility

Mercury Medical Enterprises, LLC

3 recall(s) on record — most severe on record: Class I.

Activity by year

FDA actions on record by year2015: 1 recalls; 2024: 2 recalls; 2025: 1 inspections120152016201720182019202020212022202322024120252026
  • Recalls (3)
  • Inspections (1)

Devices registered here (1)

Recalls & enforcement

  • Class IOngoing2024-12-10
    Gas powered emergency resuscitator has a circuit flow controller manufactured with an undersized spring, which may cause resuscitator not reach the high and low ends of the PIP and PEEP pressure ranges, which may cause a loss of positive pressure, impacting effective ventilation …
  • Class IOngoing2024-08-30
    Manual resuscitator circuit flow controller may come apart due to a missing manufacturing step.
  • Class IITerminated2015-10-22
    Incorrect use of T-Piece resuscitators will result in complete occlusion of the patient circuit and consequent failure to ventilate the patient.

FDA inspections (1)

  • VAI2025-12-11
    Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

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. “Mercury Medical Enterprises, LLC (FEI 1024404) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1024404-mercury-medical-enterprises-llc/

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