MCS?+ MOBILE COLLECTION SYSTEM 09000-220-E

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-30 for MCS?+ MOBILE COLLECTION SYSTEM 09000-220-E manufactured by Haemonetics Corporation.

Event Text Entries

[185672910] Donor/patient information was not provided at this time. A haemonetics field service engineer evaluated the device, determined the safety pcb board was defective and caused the error message encountered. The safety pcb was replaced and device returned to service.
Patient Sequence No: 1, Text Type: N, H10


[185672911] On (b)(6) 2018 haemonetics was notified of an adverse reaction which had occurred during the plasma donation procedure, utilizing the mcs? + mobile collection system. The plasma collection procedure was discontinued due to an error message "watchdog: id timeout". The donor then experienced a grade 3 vasovagal faint episode. The mcs? + mobile collection system collected 911ml of plasma and 500ml of saline administered. Following the administration of saline compensation, the donor made a full recovery and left the center in good health.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1219343-2018-00024
MDR Report Key9896326
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-30
Date of Report2018-07-04
Date of Event2018-06-30
Date Mfgr Received2018-07-04
Device Manufacturer Date2006-10-01
Date Added to Maude2020-03-30
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 ContactMS. JANICE KISER
Manufacturer Street125 SUMMER STREET
Manufacturer CityBOSTON, MA
Manufacturer CountryUS
Manufacturer G1HAEMONETICS CORPORATION
Manufacturer Street125 SUMMER ST
Manufacturer CityBOSTON, MA
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMCS?+ MOBILE COLLECTION SYSTEM
Generic NameMCS+,220V ENGL,LN 09000-220-E
Product CodeGKT
Date Received2020-03-30
Model Number09000-220-E
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerHAEMONETICS CORPORATION
Manufacturer Address125 SUMMER STREET BOSTON, MA US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-30

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