Beckman Coulter Inc COULTER PrepPlus and PrepPlus 2, Pipetting and Diluting station for Clinical Use Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
COULTER PrepPlus and PrepPlus 2, Pipetting and Diluting station for Clinical Use
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
All existing versions of the software. Serial numbers PrepPlus 0006026440 and above PrepPlus 2 0109079674 and above
Beckman Coulter Inc is recalling COULTER PrepPlus and PrepPlus 2, Pipetting and Diluting station for Clinical Use due to Software problem may cause the instrument to skip the probe-wash step before processing different reagents.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software problem may cause the instrument to skip the probe-wash step before processing different reagents.
Recommended Action
Per FDA guidance
The firm sent notification letter and modified operating instructions by mail on March 28, 2003.
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