CLINIMACS PLUS INSTRUMENT N/A 151-01

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 2017-09-06 for CLINIMACS PLUS INSTRUMENT N/A 151-01 manufactured by Miltenyi Biotec Gmbh.

Event Text Entries

[86574876]
Patient Sequence No: 1, Text Type: N, H10


[86574877] Clinimacs cd3/cd19 depletion runs were performed on two different clinimacs plus instruments. The instruments stopped mistream, saying process aborted. After the customer had pressed the "enter" button, the machines provided a process code.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005290010-2017-00020
MDR Report Key6847184
Report SourceCOMPANY REPRESENTATIVE
Date Received2017-09-06
Date of Report2017-09-04
Date Mfgr Received2017-08-08
Date Added to Maude2017-09-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS NANCY JOHANSEN
Manufacturer Street120 BEACON ST SUITE 200
Manufacturer CitySOMERVILLE MA 02143
Manufacturer CountryUS
Manufacturer Postal02143
Manufacturer Phone6172180062
Manufacturer G1MILTENYI BIOTEC GMBH
Manufacturer StreetFRIEDRICH-EBERT-STRASSE 68
Manufacturer CityBERGISCH GLADBACH, 51429
Manufacturer CountryGM
Manufacturer Postal Code51429
Single Use3
Remedial ActionNO
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCLINIMACS PLUS INSTRUMENT
Generic NameCLINIMACS PLUS INSTRUMENT
Product CodeOVG
Date Received2017-09-06
Model NumberN/A
Catalog Number151-01
Lot NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMILTENYI BIOTEC GMBH
Manufacturer AddressFRIEDRICH-EBERT-STRASSE 68 BERGISCH GLADBACH, 51429 GM 51429


Patients

Patient NumberTreatmentOutcomeDate
10 2017-09-06

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