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Terminated

MagNA Pure LC Instrument; catalog numbers 2236931 and 03670325001.

FDA Recall Z-1371-04 · Posted 2004-08-17

Recalling FirmRoche Diagnostics Corp.
Recall StatusTerminated
Product CodeNPQ
Date Initiated2004-08-06
Date Terminated2005-10-05
Product Quantity192

Reason for Recall

A hardware/software problem will result in low elution volumes and bias sample results for various protocols.

Firm Action

Consignees were notified via recall letter dated 8/6/04.

Root Cause

Other

Distribution Pattern

United States.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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