RegWardenFDA facility compliance records
Facility

PRECISION MEDICAL, INC.

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

Activity by year

FDA actions on record by year2015: 1 recalls; 2018: 1 inspections12015201620171201820192020202120222023202420252026
  • Recalls (1)
  • Inspections (1)

Devices registered here (1)

  • Mixer, Breathing Gases, Anesthesia Inhalation
    Product code BZR (opens in a new tab) · Class II · Anesthesiology · 21 CFR 868.5330

Recalls & enforcement

  • Class IITerminated2015-10-08
    These lots of Oxygen Dial Regulators could have the settings label off by one position. When the indicator arrow points to OFF position, the regulator is actually on the half liter setting (0.50), for the 15 liter. For the 8 liter, instead of being in the OFF position, the regula…

FDA inspections (1)

  • NAI2018-04-18
    No Action Indicated · Compliance: Devices

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. “PRECISION MEDICAL, INC. (FEI 2523148) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2523148-precision-medical-inc/

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