Roche Diagnostics Corp. MagNA Pure LC Instrument; Catalog number 2236931. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MagNA Pure LC Instrument; Catalog number 2236931.
Brand
Roche Diagnostics Corp.
Lot Codes / Batch Numbers
All systems using software version 3.0
Products Sold
All systems using software version 3.0
Roche Diagnostics Corp. is recalling MagNA Pure LC Instrument; Catalog number 2236931. due to A software bug in version 3.0 may result in prolonged mixing time, evaporation of elution volume and biased sample results for various protocols.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A software bug in version 3.0 may result in prolonged mixing time, evaporation of elution volume and biased sample results for various protocols.
Recommended Action
Per FDA guidance
An urgent product correction letter dated 6/26/03 was sent to each customer advising them not to use DNA protocols until the software update has been installed.
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