COULTER? LH 750 SLIDEMAKER 6605633

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2012-04-19 for COULTER? LH 750 SLIDEMAKER 6605633 manufactured by Beckman Coulter Inc..

Event Text Entries

[2603626] A customer contacted beckman coulter inc. (bec) reporting that when their coulter lh 750 slidemaker makes a slide, there's blood observed on the slide labels. There is an exposure control plan in place at the facility. The operators were wearing personal protective equipment (ppe) consisting of gloves and a lab coat at the time of the incident. No injury or exposure was reported. There was no impact to patient samples.
Patient Sequence No: 1, Text Type: D, B5


[9859167] A field service engineer (fse) went on-site the day of the event and found a blood spill inside the instrument and cleaned it. Fse flushed the vacuum line and drained line via rinse block assembly. Fse then cleaned the rinse block assembly and dispense probe which resolved the leak and blood on slides. This issue is likely attributed to the rinse block assembly not draining properly. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1061932-2012-01192
MDR Report Key2541305
Report Source05,06
Date Received2012-04-19
Date of Report2012-03-26
Date of Event2012-03-26
Date Mfgr Received2012-03-26
Device Manufacturer Date2009-04-01
Date Added to Maude2012-09-12
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 FDA0
Event Location0
Manufacturer ContactMS. DUNG NGUYEN
Manufacturer Street250 S KRAEMER BLVD.
Manufacturer CityBREA CA 92821
Manufacturer CountryUS
Manufacturer Postal92821
Manufacturer Phone7149614941
Manufacturer G1BECKMAN COULTER INC.
Manufacturer Street11800 SW 147TH AVENUE,
Manufacturer CityMIAMI FL 33196
Manufacturer CountryUS
Manufacturer Postal Code33196
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameCOULTER? LH 750 SLIDEMAKER
Generic NameAUTOMATED SLIDE SPINNER
Product CodeGKJ
Date Received2012-04-19
Model NumberLH 750 SLIDEMAKER
Catalog Number6605633
Lot NumberNA
ID NumberNI
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBECKMAN COULTER INC.
Manufacturer Address250 S KRAEMER BLVD. BREA CA 92821 US 92821


Patients

Patient NumberTreatmentOutcomeDate
10 2012-04-19

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.