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Terminated

Customized Automation Centrifuge, First and Second Generation.

FDA Recall Z-0975-04 · Posted 2004-07-20

Recalling FirmBeckman Coulter Inc
Recall StatusTerminated
Product CodeJQC
Date Initiated2004-05-06
Date Terminated2004-11-30
Product Quantity17

Reason for Recall

Centrifuge loss of containment with potential for injury or exposure to biohazard among lab workers.

Firm Action

Recall was by letter and by telephone. All customers have been contacted.

Root Cause

Other

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

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

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