Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Siemens RAPIDComm¿ Data Management System. The RAPIDComm¿ Data Management System Recalled by Siemens Healthcare Diagnostics Inc Due to RAPIDComm¿ 5.0 Screen Layout will display incorrect test...

Date: May 22, 2014
Company: Siemens Healthcare Diagnostics Inc
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Siemens Healthcare Diagnostics Inc directly.

Affected Products

Siemens RAPIDComm¿ Data Management System. The RAPIDComm¿ Data Management System manages the process of sending and receiving data from Siemens POC devices and hospital systems located in the hospital network,

Quantity: 6 systems

Why Was This Recalled?

RAPIDComm¿ 5.0 Screen Layout will display incorrect test names

Where Was This Sold?

This product was distributed to 2 states: OR, PA

Affected (2 states)Not affected

About Siemens Healthcare Diagnostics Inc

Siemens Healthcare Diagnostics Inc has 75 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report