INSUFFLATION/ACCESS NEEDLE 14 GAUGE * S100000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2006-11-20 for INSUFFLATION/ACCESS NEEDLE 14 GAUGE * S100000 manufactured by Ponce - Uss.

Event Text Entries

[555170] Procedure: unk. Reportedly, the veress needle was clogging and resulted in multiple attempts at placement. This resulted in subcutaneous emphysema and increased or time. The trocar was placed without problem.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2647580-2006-00486
MDR Report Key788461
Report Source05
Date Received2006-11-20
Date of Report2006-10-31
Date Mfgr Received2006-10-31
Device Manufacturer Date2005-05-01
Date Added to Maude2006-12-04
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 Location0
Manufacturer ContactJEFF DEMING - QA
Manufacturer Street195 MCDERMOTT RD.
Manufacturer CityNORTH HAVEN CT 06473
Manufacturer CountryUS
Manufacturer Postal06473
Manufacturer Phone2034926049
Manufacturer G1PONCE - USS
Manufacturer StreetSABANETAS INDUSTRIAL PARK
Manufacturer CityMERCEDITA PR 00715
Manufacturer CountryUS
Manufacturer Postal Code00715
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINSUFFLATION/ACCESS NEEDLE 14 GAUGE
Generic NameDISPOSABLE SURGICAL ACCESS DEVICE
Product CodeFHO
Date Received2006-11-20
Model Number*
Catalog NumberS100000
Lot NumberP5E444
ID Number*
Device Expiration Date2010-06-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrY
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key776167
ManufacturerPONCE - USS
Manufacturer AddressSABANETAS INDUSTRIAL PARK MERCEDITA PR 00715 US
Baseline Brand NameINSUFFLATION/ACCESS NEEDLE 14G
Baseline Generic NameSURGICAL ACCESS NEEDLE
Baseline Model NoNA
Baseline Catalog NoS100000
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2006-11-20

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.