Facility

MIDMARK CORP.

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

Key facts

4recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3043668257
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	9987 Carver Rd Ste 310 Blue Ash, OH, US 45242
Registration status	Active · expires 2026
Parent company	MIDMARK CORP. (owner-operator 9915004)
Brand names	Midmark IQecg Electrocardiograph

Activity by year

Recalls (4)

Devices registered here (1)

Electrocardiograph
Product code DPS (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.2340

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. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “MIDMARK CORP. (FEI 3043668257) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3043668257-midmark-corp/

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