GETINGE recalls PulsioFlex Monitoring System (model PC400 3 R0) with internal error message 'restart or service' that may cause incorrect readings. Affected units have specific serial numbers.
The monitor displays an error message . The error message states "internal error restart or service".
GETINGE is recalling a specific model of hospital monitor that displays an error message indicating it needs service. This could lead to inaccurate patient monitoring readings if the monitor is used without proper maintenance.
The monitor shows an error message 'internal error restart or service' when it has a problem. This could cause incorrect patient readings if the monitor is used without proper service. The error does not indicate immediate danger but requires attention to maintain accurate monitoring.
Hospital staff and patients using the PulsioFlex Monitoring System with specific serial numbers. Those in medical settings where cardiovascular monitoring is critical are most at risk.
Check for the model number PC400 3 R0 and serial numbers starting with K17400011005 or K17400011065 or K17400011082 or K17400011086 or K17400011097 or K17400011107 or L17400011267. The monitor is used in hospitals for cardiovascular monitoring.
Look for the error message 'internal error restart or service' on the monitor display.
The monitor displays an error message 'internal error restart or service' which may cause inaccurate patient readings if not addressed.
Check if the monitor needs service by contacting GETINGE support or following the recall instructions.
Affected units have specific serial numbers: K17400011005, K17400011065, K17400011082, K17400011086, K17400011097, K17400011107, or L17400011267.
We’ve drafted a message you can send GETINGE to request your refund or repair — edit it as you like.
Subject: Recall Z-2077-2019 — GETINGE GETINGE Hello, I own a GETINGE that is covered by recall Z-2077-2019 from GETINGE. 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.
