Z-0570-03

AcT 5 diff Cap Pierce Hematology Analyzer 864.5220 Automated differential cell counter

Name: Z-0570-03 AcT 5 diff Cap Pierce Hematology Analyzer 864.5220 Automated differential cell counter
Creator: Beckman Coulter Inc
Published: 2003-01-20
License: https://open.fda.gov/license/

Siemens Healthcare Diagnostics Inc. / initiated 2003-01-20 / Terminated

FDA source

Beckman Coulter Inc began a recall of AcT 5 diff Cap Pierce Hematology Analyzer 864.5220 Automated differential cell counter on 2003-01-20. The reason FDA records is "Failure to cycle properly ammong samples". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0570-03
Status: Terminated
Initiated: 2003-01-20
Posted: 2003-02-25
Terminated: 2003-07-26
Recalling firm: Siemens Healthcare Diagnostics Inc.
Product: AcT 5 diff Cap Pierce Hematology Analyzer 864.5220 Automated differential cell counter
Reason for recall: Failure to cycle properly ammong samples.
FDA root cause: Other
Action: Customers were sent a letter dated January 20, 2003 that describes this situation and provides modified operating instructions to prevent the occurence.
Quantity in commerce: 351
Distribution: US and Canada
Product codes and lots: Not applicaable.

K003677Class IIAbx Pentra 60C+ Hematology AnalyzerAbx Diagnostics / cleared 2000-12-26

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)