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Terminated

Coulter LH 700 Series Hematology Analyzers

FDA Recall Z-0541-03 · Posted 2003-02-05

Recalling FirmBeckman Coulter Inc
Recall StatusTerminated
Product CodeGKZ
Date Initiated2003-01-10
Date Terminated2003-07-26
Product Quantity210

Reason for Recall

Biohazard situation exists for users.

Firm Action

Customers were sent letters instructing them to remove and replace affected pages in their manuals. Letters were sent January 10, 2003.

Root Cause

Other

Distribution Pattern

Nationwide and Canada.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K011342COULTER LH 750 HEMATOLOGY ANALYZER, MODEL 6605632Beckman Coulter, Inc. · 2001-07-09

Official Source

View FDA Recall →

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

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