ABX Diagnostics Inc PENTRA 120 and PENTRA 120 Retic Hematology Analyzer Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
PENTRA 120 and PENTRA 120 Retic Hematology Analyzer
Brand
ABX Diagnostics Inc
Lot Codes / Batch Numbers
Any instrument which is not equipped with v4.55 or above will be upgraded.
Products Sold
Any instrument which is not equipped with v4.55 or above will be upgraded.
ABX Diagnostics Inc is recalling PENTRA 120 and PENTRA 120 Retic Hematology Analyzer due to Power failure having impact on software.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Power failure having impact on software.
Recommended Action
Per FDA guidance
Firm sent a notification / recall letter and response card dated June 24,2004 and promised to provide software shortly.
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