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FDA (Device enforcement)Recalled 2024-04-22class ii

GE Medical Systems Information Technologies Inc: Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX electrophysiology recording system and ComboLab AltiX hemodynamic and electrophysiology rec

Hazard

Capacitors in certain Prucka 3 Amplifiers used with CardioLab / ComboLab systems could fail resulting in transient oscillations on the display and inability to view surface and intracardiac ECG waveforms.

Details from the source

Reason for recall: Capacitors in certain Prucka 3 Amplifiers used with CardioLab / ComboLab systems could fail resulting in transient oscillations on the display and inability to view surface and intracardiac ECG waveforms. Distribution: Worldwide - US Nationwide distribution in the states of AK, AZ, CA, CO, FL, GA, IL, KY, MA, ME, MN, MO, NC, NJ, NY, OH, OR, PA, TN, TX, and WA. The countries of Belgium, Canada, Czech Republic, France, Germany, Ireland, Israel, Italy, Japan, Republic of Korea, and Singapore. Quantity: 145 units Lot/code info: UDI N/A for the Prucka 3 Amplifier-not a medical device. CardioLab and ComboLab Systems GTIN #00195278507044 and #00195278507051. Prucka 3 Amplifier serial numbers: SVS23400020SA, SVS23400024SA, SVS23360017SA, SVS23400003SA, SVS23470003SA, SVS23350005SA, SVS23330008SA, SVS23350001SA, SVS23350003SA, SVS23360018SA, SVS23520022SA, SVS23350008SA, SVS23280009SA, SVS23350021SA, SVS23470016SA, SVS23470010SA, SVS23360013SA, SVS23280002SA, SVS23400026SA, SVS23400039SA, SVS23400021SA, SVS23330006SA, SVS23360014SA, SVS23360016SA, SVS23460020SA, SVS23470022SA, SVS23480007SA, SVS23360010SA, SVS23350024SA, SVS24020002SA, SVS24020004SA, SVS24020005SA, SVS24020006SA, SVS24020007SA, SVS24020011SA, SVS23460002SA, SVS23350004SA, SVS23350006SA, SVS23350007SA, SVS23480003SA, SVS23400008SA, SVS23210005SA, SVS23360007SA, SVS23360002SA, SVS23360012SA, SVS23470004SA, SVS23520018SA, SVS23520020SA, SVS24020016SA, SVS23460001SA, SVS23470006SA, SVS23470008SA, SVS23350002SA, SVS23350009SA, SVS23350025SA, SVS23360003SA, SVS23360005SA, SVS23360006SA, SVS23360011SA, SVS23400023SA, SVS23400030SA, SVS23400031SA, SVS23400032SA, SVS23400037SA, SVS23400038SA, SVS23460007SA, SVS23400015SA, SVS23350011SA, SVS23350017SA, SVS23470017SA, SVS23470018SA, SVS23470020SA, SVS23460013SA, SVS23460014SA, SVS23480002SA, SVS23480005SA, SVS23480010SA, SVS23480011SA, SVS23480013SA, SVS23480015SA, SVS23520012SA, SVS23280008SA, SVS23290004SA, SVS23330004SA, SVS23350014SA, SVS23350022SA, SVS23350023SA, SVS23460006SA, SVS23400022SA,

UPC codes

00195278507044, 00195278507051

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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