THINPREP 5000 PROCESSOR

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-06-17 for THINPREP 5000 PROCESSOR manufactured by Hologic, Inc.

Event Text Entries

[47608305] A customer in (b)(6) reported one incident where their thinprep 5000 processor with autoloader etched a slide with a mismatched number; without producing an error code. The customer confirmed that the sample was found and reprocessed. The barcode produced was correct and matched the vial id upon processing the sample the second time. Hologic's field service engineer (fse) was dispatched to customer's site. Fse performed tsb-00882. Fse followed up with customer and confirmed instrument is operational since tsb was performed. Although no patients needed to be recalled as a result of this incident this is a reportable event since the instrument did not perform as intended.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1222780-2016-00139
MDR Report Key5732114
Date Received2016-06-17
Date of Report2016-06-15
Date Mfgr Received2016-05-25
Date Added to Maude2016-06-17
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactEVA MAXWELL
Manufacturer Street250 CAMPUS DRIVE
Manufacturer CityMARLBOROUGH MA 01752
Manufacturer CountryUS
Manufacturer Postal01752
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTHINPREP 5000 PROCESSOR
Generic NameTHINPREP 5000 PROCESSOR
Product CodeMKQ
Date Received2016-06-17
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerHOLOGIC, INC
Manufacturer Address250 CAMPUS DRIVE MARLBOROUGH MA 01752 US 01752


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2016-06-17

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