RegWardenFDA facility compliance records
Company

MIDMARK CORP.

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

Recalls by year

FDA actions on record by year2013: 1 recalls; 2014: 1 recalls; 2026: 2 recalls1’131’14’15’16’17’18’19’20’21’22’23’24’252’26
  • Recalls (4)

Registered facilities (2)

Recalls & enforcement

  • Class IIOngoing2026-08-21
    A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
  • Class IIOngoing2026-07-20
    A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.
  • Class IITerminated2014-09-04
    Failure of the primary collimator may result in unintentional movement of the device. The unintentional movement will not result in the generation of an error message.
  • Class IITerminated2013-09-20
    An error was identified in the Real Time Controller (RTC) firmware versions 3.0, 3.1, 3.2, and 3.3 used in Vantage Panoramic X-Ray systems. The error may cause the column of the Vantage Panoramic X-Ray unit to continue moving vertically despite the release of the movement control…

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. “MIDMARK CORP. — 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-9915004-midmark-corp/

Not open yet

Alerts for MIDMARK CORP.

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.