RegWardenFDA facility compliance records
Facility

ESTILL MEDICAL TECHNOLOGIES, INC.

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

Activity by year

FDA actions on record by year2014: 1 recalls; 2017: 1 inspections1’14’15’161’17’18’19’20’21’22’23’24’25’26
  • Recalls (1)
  • Inspections (1)

Devices registered here (2)

  • Warmer, Blood, Non-Electromagnetic Radiation
    Product code BSB (opens in a new tab) · Class II · Hematology · 21 CFR 864.9205
  • Warmer, Thermal, Infusion Fluid
    Product code LGZ (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5725

Recalls & enforcement

  • Class IITerminated2014-07-25
    Estill has discovered that a fully discharged Ultra Battery 1 (TA-UB1) will reach 96.9% of its capacity during a 60 minute charging period. If you have a fully discharged Ultra Battery 1 (TA-UB1), in order to achieve a 100% of charge capacity you should charge it for a period of…

FDA inspections (1)

  • NAI2017-12-20
    No Action Indicated · Compliance: Devices; Postmarket Assurance: 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. “ESTILL MEDICAL TECHNOLOGIES, INC. (FEI 3002587972) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3002587972-estill-medical-technologies-inc/

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