Beckman Coulter Inc UniCel DxC 600i, Part Numbers: A25638, A25639, Beckman Coulter, Inc. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
UniCel DxC 600i, Part Numbers: A25638, A25639, Beckman Coulter, Inc.
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
Part Numbers: A25638, A25639. All serial numbers. All software versions
Products Sold
Part Numbers: A25638, A25639. All serial numbers. All software versions
Beckman Coulter Inc is recalling UniCel DxC 600i, Part Numbers: A25638, A25639, Beckman Coulter, Inc. due to Intermittent Failure of Stirrer Motor-Beckman Coulter has determined that incorrect Glucose results on LX20 or DxC instruments have been related to an. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Intermittent Failure of Stirrer Motor-Beckman Coulter has determined that incorrect Glucose results on LX20 or DxC instruments have been related to an intermittent failure of the stirrer motor. -Stirrer motors can stall without any flags or motion errors. -If a stall occurs during a GLUm test near the time of sample inject, results may be affected. -Affected GLUm results may be high or low.
Recommended Action
Per FDA guidance
GLUm stir motors greater than one year old were replaced. Replacements began April 5, 2007. Based on the Risk Assessment, BCI decided that Customer Notification is not needed. GLUm stir motors greater than one year old will be replaced on high volume LX/DxC systems by 3rd quarter of 2007. Replacements began April 5, 2007. A new stirrer design is being developed and is expected to be available before 4th quarter of 2007. Implementation Strategy of Stock Control: 1. A Stop Ship was not necessary based on risk assessment. The possibility of stirrer motor failure may increase with time and duty cycles. Systems running a high volume of tests may have a greater likelihood of exhibiting stirrer motor failure with motors greater than one year old. 2. New Customers were placed on a preventative maintenance plan to have their motor replaced at one year cycle. Completed 3. A Technical Update was issued to notify Hotline and Field Service Personnel of the issues.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026