RecallDepth

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

This recall has been completed (originally issued October 31, 2024).

Company
Accriva Diagnostics, Inc.
Recall Initiated
September 27, 2024
Posted
October 31, 2024
Recall Number
Z-0279-2025
Quantity
1
Firm Location
San Diego, CA
Official Source
View on FDA website ↗

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.

Distribution

US: AZ

Lot / Code Info

UDI-DI: 10711234530023. Serial Number: 6824

Root Cause

Process change control

Action Taken

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 techsupport.na@werfen.com.

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