VIAL-MATE RECONSTITUTION DEVICE 2B8071

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-31 for VIAL-MATE RECONSTITUTION DEVICE 2B8071 manufactured by Baxter Healthcare Corporation.

Event Text Entries

[185735057] (b)(6). Should additional relevant information become available, a supplemental report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[185735058] It was reported that a vial-mate reconstitution device was leaking from the intersection of the blue port and white gripper. This was further described as? Flange of blue port not flush with medication bag, blue port and white gripper separated after reconstitution.? There was no report of patient injury or medical intervention associated with this event. No additional information is available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1416980-2020-01867
MDR Report Key9903675
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-31
Date of Report2020-03-31
Date of Event2020-03-04
Date Mfgr Received2020-03-06
Date Added to Maude2020-03-31
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 Street25212 W. ILLINOIS ROUTE 120
Manufacturer CityROUND LAKE IL 60073
Manufacturer CountryUS
Manufacturer Postal60073
Manufacturer Phone2242702068
Manufacturer G1BAXTER HEALTHCARE - CLEVELAND
Manufacturer Street911 HIGHWAY 61 NORTH PO BOX 1058
Manufacturer CityCLEVELAND MS 38732
Manufacturer CountryUS
Manufacturer Postal Code38732
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVIAL-MATE RECONSTITUTION DEVICE
Generic NameSET, I.V. FLUID TRANSFER
Product CodeLHI
Date Received2020-03-31
Model NumberNA
Catalog Number2B8071
Lot NumberASKU
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBAXTER HEALTHCARE CORPORATION
Manufacturer AddressDEERFIELD IL


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-31

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