EXTRACTION BAG FOR MIS IPN004939 332800-000010

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-03-12 for EXTRACTION BAG FOR MIS IPN004939 332800-000010 manufactured by Teleflex Medical.

Event Text Entries

[183124161] (b)(4). The device has not been returned for investigation. Teleflex will continue to monitor and trend related events.
Patient Sequence No: 1, Text Type: N, H10


[183124162] It was reported that the extraction bag tore while removing an appendectomy piece from the patient. This piece got stuck in the umbilical of the patient. It's the 4th incident we had with extraction bag since 2019. We had to enlarge the patient's umbilical hole to extract the piece and then wash/rinse with betadine.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006425876-2020-00238
MDR Report Key9824076
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2020-03-12
Date of Report2020-02-20
Date of Event2020-02-19
Date Mfgr Received2020-02-20
Device Manufacturer Date2020-01-17
Date Added to Maude2020-03-12
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 ContactEFFIE JEFFERSON
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194332672
Manufacturer G1ARROW INTERNATIONAL CR, A.S.
Manufacturer StreetJAMSKA 2359/47
Manufacturer CityZDAR NAD SAZAVOU 591 01
Manufacturer CountryEZ
Manufacturer Postal Code591 01
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEXTRACTION BAG FOR MIS
Product CodeKGY
Date Received2020-03-12
Model NumberIPN004939
Catalog Number332800-000010
Lot Number71F20A0558
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressATHLONE


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-12

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