GE Medical recalls Prucka 3 Amplifier Model P1801PA used with CardioLab/ComboLab systems due to capacitor failure causing display oscillations and ECG waveform issues. Affected units have specific serial numbers.
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.
GE Medical is recalling Prucka 3 Amplifiers with model #P1801PA that are used with CardioLab or ComboLab systems. These amplifiers can have capacitors fail, causing temporary display oscillations and making it impossible to view ECG waveforms during medical procedures.
Capacitors in certain Prucka 3 Amplifiers used with CardioLab or ComboLab systems can fail, causing temporary display oscillations and preventing healthcare workers from viewing surface and intracardiac ECG waveforms during medical procedures.
Healthcare professionals using the Prucka 3 Amplifier with CardioLab or ComboLab systems are most at risk. Affected units have specific serial numbers listed in the recall notice.
Check if your Prucka 3 Amplifier has model #P1801PA and serial numbers listed in the recall notice. The amplifier is used with CardioLab AltiX or ComboLab AltiX systems. The serial numbers start with 'SVS23' followed by specific digits.
Look for the serial number on your Prucka 3 Amplifier, which starts with 'SVS23' followed by specific digits.
The recall states that capacitors in certain units can fail, causing display issues. Affected units should be checked against the list of serial numbers provided.
Check if your Prucka 3 Amplifier has model #P1801PA and a serial number starting with 'SVS23' followed by specific digits listed in the recall notice.
The recall does not specify a remedy, so affected units should be checked against the list of serial numbers provided. GE Medical has not issued a repair or replacement solution.
We’ve drafted a message you can send GE Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2258-2024 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-2258-2024 from GE Medical Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
