Dna Probe, Trichomonas Vaginalis

FDA product code MJK · Class 1 · Microbiology

Registered devices

Adverse events

Recalls

510(k) clearances

Devices with this code

Date	Firm	Reason
2008-08-28	Physio Control, Inc.	This recall is being conducted due to the device being configured with the incorrect software for semi-automatic instead of fully automatic use. When the device
2007-04-27	Medtronic Emergency Response Systems, Inc.	White Screen Lock up: LifePak 20 defibrillators with software version 48 or version 52 may experience an intermittent timing issue during the power on sequence.
2007-03-30	Medtronic Emergency Response Systems, Inc.	Defibrillator internal battery cell may contain a short which could reduce battery capacity and cause the device to shut down without warning while operating on
2007-03-30	Medtronic Emergency Response Systems, Inc.	Defibrillator internal battery cell may contain a short which could reduce battery capacity and cause the device to shut down without warning while operating on
2006-11-15	MRL, Inc., A Welch Allyn Company	Shock Delay:The monitor-defibrillator may display an 'ECG Comm' error message on the display during use, which may prevent or cause an unacceptable delay the d
2006-06-30	MRL, Inc., A Welch Allyn Company	The Welch Allyn PIC 50 Defibrillators may display a 'Defib Comm' or 'Pace Comm' error message on the device display during use which may result in a terminal fa

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.