NEOCONNECT ORAL / ENTERAL SYRINGE NM-S35NC

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-12-15 for NEOCONNECT ORAL / ENTERAL SYRINGE NM-S35NC manufactured by Neomed, Inc..

Event Text Entries

[94957217]
Patient Sequence No: 1, Text Type: N, H10


[94957218] Nurse received 35 ml enteral feeding syringe from the infant formula room. Rn found sealing cap difficult to remove. While trying to twist cap from syringe barrel, the syringe connector snapped off of the syringe barrel. The nurse transferred the breast milk to another syringe and proceeded with the feeding. Damaged syringe removed and sent to biomedical for evaluation. Manufacturer response for enteral syringe, enfit compliant, neoconnect (per site reporter): awaiting response.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number7120463
MDR Report Key7120463
Date Received2017-12-15
Date of Report2017-12-12
Date of Event2017-11-15
Report Date2017-12-12
Date Reported to FDA2017-12-12
Date Reported to Mfgr2017-12-12
Date Added to Maude2017-12-15
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNEOCONNECT ORAL / ENTERAL SYRINGE
Generic NameENTERAL SYRINGES WITH ENTERAL SPECIFIC CONNECTORS
Product CodePNR
Date Received2017-12-15
Model NumberNM-S35NC
Catalog NumberNM-S35NC
OperatorNURSE
Device Availability*
Device Age1 DY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerNEOMED, INC.
Manufacturer Address100 LONDONDERRY COURT SUITE 112 WOODSTOCK GA 30188 US 30188


Patients

Patient NumberTreatmentOutcomeDate
10 2017-12-15

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