FDA Adverse Event Other Summary report: N

THE IMAGER

MDR report key: 2310384 · Received October 23, 2011

Report

Report Number
MW5022818
Event Type
Other
Date Received
October 23, 2011
Report Date
October 23, 2011
Manufacturer
HOLOGIC CORPORATION
Product Code
MKQ
Report Source
Voluntary report
Reporter Location
OH, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

HOLOGIC IMAGER MISSED KOILOCYTIC CELLS ON PAP TEST. RESULT WAS CALLED (B)(6).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 THE IMAGER IMAGER MKQ HOLOGIC CORPORATION

Patients

Seq Age Sex Outcome Treatment
1 47 YR Other