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Terminated

Synchron LX Systems Primary Tube Sample Template (a piece of ''labeling'' for use with the Synchron LX 20 and LX 20 Pro systems). Part Number: 967178

FDA Recall Z-1077-03 · Posted 2003-08-06

Recalling FirmBeckman Coulter Inc
Recall StatusTerminated
Date Initiated2003-06-19
Date Terminated2004-12-01
Product Quantity502

Reason for Recall

Dead volume on sight gauge for the Synchron LX 20 and LX 20 Pro Systems not stated, which may result in instrument error.

Firm Action

A revised template with a recall letter was sent to customers with a response request on 19 June 2003.

Root Cause

Other

Distribution Pattern

USA and Canada.

Official Source

View FDA Recall →

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

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