FDAFDA · Food and drugs·Recall number Z-2258-2024
Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX electrophysiology recording system and ComboLab AltiX hemodynamic and electrophysiology recording system; and Field Replacement Units spare part #5875569 (Assy CLABIII AMP 128CH 100-240V 50-60HZ).
Published July 10, 2024 · Recall initiated: April 22, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the 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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- GE Medical Systems Information Technologies Inc
- Distributor
- 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.
- Lot
- 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, SVS23350012SA, SVS23350016SA, SVS23480004SA, SVS23470007SA, SVS23400025SA, SVS23460003SA, SVS23460004SA, SVS23350015SA, SVS23320002SA, SVS23470013SA, SVS23350020SA, SVS23330005SA, SVS23470009SA, SVS23470011SA, SVS23470019SA, SVS23470012SA, SVS23460016SA, SVS23290001SA, SVS23350013SA, SVS23460017SA, SVS23480012SA, SVS23480016SA, SVS23330007SA, SVS23360008SA, SVS23360020SA, SVS23400005SA, SVS23400009SA, SVS23400010SA, SVS23400019SA, SVS23460008SA, SVS23280005SA, SVS23400004SA, SVS23460005SA, SVS23400034SA, SVS23400035SA, SVS23400036SA, SVS23400033SA, SVS23400018SA, SVS23470005SA, SVS23400028SA, SVS23400029SA, SVS23360019SA, SVS23400002SA, SVS23360004SA, SVS23400007SA, SVS23400011SA, SVS23400006SA, SVS23350018SA, SVS23330003SA, SVS23290003SA, SVS23290002SA, SVS23330009SA, SVS23350019SA, SVS23360015SA, SVS23470001SA, and SVS23470002SA.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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