Accriva recalls AVOXimeter 1000E bedside blood oxygen monitors that may show falsely high oxygen levels, risking incorrect patient care. Affected units have specific product numbers and serial numbers.
Values used to calibrate whole blood oximeter instruments were observed to be higher than normal, which may result in incorrect patient results where oxygen levels are higher than actual results, which may lead to patient care mismanagement requiring medical intervention.
Accriva is recalling its AVOXimeter 1000E blood oxygen monitors because they may show higher oxygen levels than actual, potentially leading to incorrect patient care decisions. This could cause unnecessary medical interventions if healthcare providers rely on the device's readings.
The device may display oxygen levels higher than actual, which could lead to healthcare providers taking unnecessary medical actions. This might cause patients to receive treatments they don't need, though serious harm is unlikely.
Healthcare providers using the AVOXimeter 1000E for patient oxygen monitoring are most at risk. Patients using the device at home may also be affected if they rely on its readings.
Check for product number AVOX1000E and serial number 6824 on the device. The device is a battery-operated bedside blood oxygen monitor sold by Accriva Diagnostics.
Look for product number AVOX1000E and serial number 6824 on the device.
The AVOXimeter 1000E may show higher oxygen levels than actual, which could lead to incorrect patient care decisions.
Check for product number AVOX1000E and serial number 6824. The recall does not require immediate action beyond checking the device details.
The recall states the device may cause incorrect patient care, but it does not mention risks of serious injury or death.
We’ve drafted a message you can send Accriva to request your refund or repair — edit it as you like.
Subject: Recall Z-0279-2025 — Accriva Accriva Hello, I own a Accriva that is covered by recall Z-0279-2025 from Accriva. 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.
