Roche Diagnostics Corp. MagNA Pure LC Instrument; catalog numbers 2236931 and 03670325001. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MagNA Pure LC Instrument; catalog numbers 2236931 and 03670325001.
Brand
Roche Diagnostics Corp.
Lot Codes / Batch Numbers
All units using software version 3.03.
Products Sold
All units using software version 3.03.
Roche Diagnostics Corp. is recalling MagNA Pure LC Instrument; catalog numbers 2236931 and 03670325001. due to A hardware/software problem will result in low elution volumes and bias 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 hardware/software problem will result in low elution volumes and bias sample results for various protocols.
Recommended Action
Per FDA guidance
Consignees were notified via recall letter dated 8/6/04.
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