PNEUMOPERITONEUM INSUFFLATION NEEDLE - 120MM LENGTH PN120

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-07-31 for PNEUMOPERITONEUM INSUFFLATION NEEDLE - 120MM LENGTH PN120 manufactured by Ethicon Endo-surgery, Llc..

Event Text Entries

[23230282] (b)(4). Information not available, device not returned for analysis. Should the information be provided later, a supplemental medwatch will be sent.
Patient Sequence No: 1, Text Type: N, H10


[23230283] It was reported that during a laparoscopic gynecologic procedure, as the device entered the abdomen, the first click was heard but there was no subsequent second click and the sheath had not retracted back to cover the needle tip. It is not known how the procedure was completed. There were no adverse consequences for the patient reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005075853-2015-04757
MDR Report Key4957862
Date Received2015-07-31
Date of Report2015-07-21
Date of Event2015-07-17
Date Mfgr Received2015-07-20
Date Added to Maude2015-07-31
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 ContactMILTON GARRETT
Manufacturer Street4545 CREEK ROAD ML 120A
Manufacturer CityCINCINNATI OH 45242
Manufacturer CountryUS
Manufacturer Postal45242
Manufacturer Phone5133378865
Manufacturer G1ETHICON ENDO-SURGERY, LLC
Manufacturer Street475 CALLE C
Manufacturer CityGUAYNABO PR 00969
Manufacturer Postal Code00969
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report0

Device Details

Brand NamePNEUMOPERITONEUM INSUFFLATION NEEDLE - 120MM LENGTH
Product CodeFDP
Date Received2015-07-31
Model NumberNA
Catalog NumberPN120
Lot NumberM4HD0G
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerETHICON ENDO-SURGERY, LLC.
Manufacturer Address475 CALLE C GUAYNABO PR 00969 00969


Patients

Patient NumberTreatmentOutcomeDate
10 2015-07-31

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