MINIBAG PLUS CONTAINER 2C4950

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-01-28 for MINIBAG PLUS CONTAINER 2C4950 manufactured by Baxter Healthcare - Cleveland.

Event Text Entries

[134444946] Common device name: equipment, laboratory, general purpose, labeled or promoted for a specific medical use. A batch review was conducted and there were no deviations found related to this reported condition during the manufacture of this lot. The device was not received for evaluation; therefore, a device analysis could not be completed. Should additional relevant information become available, a supplemental report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[134444947] This report summarizes 1 malfunction events. It was reported that rust was observed on a mini-bag plus container/vial docking tool during compounding. There was no patient involvement. No additional information is available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1416980-2019-00331
MDR Report Key8283739
Date Received2019-01-28
Date of Report2019-01-28
Date Mfgr Received2018-12-31
Date Added to Maude2019-01-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
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 Report0

Device Details

Brand NameMINIBAG PLUS CONTAINER
Generic NameSEE H10
Product CodeLXG
Date Received2019-01-28
Model NumberNA
Catalog Number2C4950
Lot NumberGD898916
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerBAXTER HEALTHCARE - CLEVELAND
Manufacturer AddressCLEVELAND MS


Patients

Patient NumberTreatmentOutcomeDate
10 2019-01-28

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