Z-1041-05

Beckman Coulter 1500 Series Hematology Automation System; Part Number: 988609 (LH Basic Uint) 988610 (LH...

Name: Z-1041-05 Beckman Coulter 1500 Series Hematology Automation System; Part Number: 988609 (LH Basic Uint) 988610 (LH...
Creator: Beckman Coulter Inc
Published: 2005-06-20
License: https://open.fda.gov/license/

Siemens Healthcare Diagnostics Inc. / initiated 2005-06-20 / Terminated

FDA source

Beckman Coulter Inc began a recall of Beckman Coulter 1500 Series Hematology Automation System; Part Number: 988609 (LH Basic Uint) 988610 (LH Connection Unit) on 2005-06-20. The reason FDA records is "Risk of injury to workers due to mechanical or electrical hazards". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1041-05
Status: Terminated
Initiated: 2005-06-20
Posted: 2005-07-22
Terminated: 2012-03-07
Recalling firm: Siemens Healthcare Diagnostics Inc.
Product: Beckman Coulter 1500 Series Hematology Automation System; Part Number: 988609 (LH Basic Uint) 988610 (LH Connection Unit)
Product code: GKZ Counter, Differential Cell
Reason for recall: Risk of injury to workers due to mechanical or electrical hazards.
FDA root cause: Other
Action: Letters were sent advising of the hazard during the week of June 20, 2005 it stated that the units would be upgraded by appointment.
Quantity in commerce: 34
Distribution: USA and Canada
Product codes and lots: NA

Product code GKZ

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)