B. BRAUN TUBING

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-03-28 for B. BRAUN TUBING manufactured by B. Braun Medical Inc..

Event Text Entries

[140445024] Primary rn was hanging chemo on pt and as soon as equashield luer locked, chemo stopped immediately. There was an equashield on tubing prior, but rn replaced a new one before hanging chemo. Therefore, the leak came after the new equashield was replaced. It was not considered a chemo spill because it was less than 5ml. Tubing was changed and a new equashield replaced before therapy started and there was no incident. Pt free from harm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5085305
MDR Report Key8464387
Date Received2019-03-28
Date of Report2019-03-20
Date of Event2019-03-10
Date Added to Maude2019-03-29
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
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
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Sequence Number: 1

Brand NameB. BRAUN TUBING
Generic NameTUBING, FLUID DELIVERY
Product CodeFPK
Date Received2019-03-28
Lot Number0061656319
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerB. BRAUN MEDICAL INC.

Device Sequence Number: 2

Brand NameEQUASHIELD LUER LOCK
Generic NameCLOSED ANTICOPLASTIC AND HAZARDOUS DRUG RECONSTITUTION AND TRANSFER SYSTEM
Product CodeONB
Date Received2019-03-28
Lot Number1820415
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrI
Device Sequence No2
Device Event Key0
ManufacturerEQUASHIELD LLC


Patients

Patient NumberTreatmentOutcomeDate
10 2019-03-28

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