ABX Diagnostics Inc ABX Diagnostices Pentra 60C+ Hematology Analyzer Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ABX Diagnostices Pentra 60C+ Hematology Analyzer
Brand
ABX Diagnostics Inc
Lot Codes / Batch Numbers
Software versions of up to 1.7
Products Sold
Software versions of up to 1.7
ABX Diagnostics Inc is recalling ABX Diagnostices Pentra 60C+ Hematology Analyzer due to Instrument fails to obtain correct patient information/results due to malfunction of the equipment's sample door.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Instrument fails to obtain correct patient information/results due to malfunction of the equipment's sample door.
Recommended Action
Per FDA guidance
The firm distributed a 'Product Advisory Note' on June 5, 2003 by mail which includes instructions on how to avoid problems. It also mentions a new software release which will fix the problem.
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