FDA Recall Completed

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

Recall: Z-0279-2025 · Initiated September 27, 2024

Recall

Recall Number
Z-0279-2025
Event Number
95497
Firm
Accriva Diagnostics, Inc.
FEI Number
2250033
Product Code
DQA
Status
Completed
Root Cause
Process change control
Initiated
September 27, 2024
Posted
October 31, 2024
Address
6260 Sequence Dr, San Diego, CA, 92121-4358

Description

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

Reason

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.

Action

On 9/27/24, a recall notice was sent to a customer informing them to do the following: 1) This recall notice should be shared with anyone who needs to be aware within your organization and forwarded to any organization where the potentially affected device has been transferred.. 2. Call Technical Support 1-800-678-0710 to initiate a Service Call and Returned Material Authorization 3. Complete and return the customer response form via email to For technical questions contact Technical Support at the number above or email [email protected].

Distribution

US: AZ

Quantity

1