PlainRecalls
FDA Devices Moderate Class II Completed

AVOXimeter 1000E, Product Number: AVOX1000E. The AVOXimeter 1000E is a battery-operated bedside whole blood oximeter.

Reported: November 6, 2024 Initiated: September 27, 2024 #Z-0279-2025

Product Description

AVOXimeter 1000E, Product Number: AVOX1000E. The AVOXimeter 1000E is a battery-operated bedside whole blood oximeter.

Reason for Recall

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.

Details

Recalling Firm
Accriva Diagnostics, Inc.
Units Affected
1
Distribution
US: AZ
Location
San Diego, CA

Frequently Asked Questions

What product was recalled?
AVOXimeter 1000E, Product Number: AVOX1000E. The AVOXimeter 1000E is a battery-operated bedside whole blood oximeter.. Recalled by Accriva Diagnostics, Inc.. Units affected: 1.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 6, 2024. Severity: Moderate. Recall number: Z-0279-2025.