Medical Device Recall: Z-0039-04

FDA Recalls dataset · Firm: Beckman Coulter Inc · Status: Terminated

Recall Action Class: N/A Date Initiated: 2003-09-08 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0039-04.

Recall Res Number
Z-0039-04
Recalling Firm / Manufacturer
FEI Number
2050012
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2003-09-08
Date Posted
2003-10-15
Date Terminated
2004-03-30
Product Code
GKZ
Event Number
27251
Product Quantity
36
Product Description Coulter AcT 5diff Open Vial Hematology Analyzers Part Numbers: 6605580, 6605581, 6605604

Reason for Recall Samples with high fat content will not count platelets accurately.

Action Details Firm issued an advisory letter to users to retain as part of the Quality Manual for the instruments. It cautions to check specimens for interfering lipemia. Letter was sent 9/8/2003.

Distribution Pattern United States and Canada

Code Information / Serial Numbers All instruements are affected.

Related Establishments / Registrations

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