SUTURE UNKNOWN

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-04-26 for SUTURE UNKNOWN manufactured by Ethicon Inc..

Event Text Entries

[106699787] (b)(4). To date the device has not been returned. If the device or further details are received at a later date a supplemental medwatch will be sent.
Patient Sequence No: 1, Text Type: N, H10


[106699788] It was reported that the patient underwent an unknown procedure on an unknown date and suture was used. During the procedure, the foil pack cut the fingers of the or staff, opening the skin to infection. The cut was treated with topical skin adhesive. The injury is reported to be healed. No additional information was available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2210968-2018-72377
MDR Report Key7466997
Date Received2018-04-26
Date of Report2018-04-14
Date of Event2018-01-01
Date Mfgr Received2018-04-14
Date Added to Maude2018-04-26
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 ContactDARLENE KYLE
Manufacturer StreetP.O. BOX 151, ROUTE 22 WEST
Manufacturer CitySOMERVILLE NJ 088760151
Manufacturer CountryUS
Manufacturer Postal088760151
Manufacturer Phone9082182792
Manufacturer G1ETHICON INC.
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSUTURE UNKNOWN
Generic NameSUTURE, NONABSORBABLE
Product CodeGAO
Date Received2018-04-26
Catalog NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerETHICON INC.
Manufacturer AddressP.O. BOX 151, ROUTE 22 WEST SOMERVILLE NJ 088760151 US 088760151


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-04-26

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