UNKNOWN SUTURE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2017-10-02 for UNKNOWN SUTURE manufactured by Ethicon Inc..

Event Text Entries

[88073263] Attempts have been made to retrieve the device. To date the device has not been returned. If the device or further details are received at the later date a supplemental medwatch will be sent. Attempts are being made to obtain the additional information. To date no response has been provided. If further details are received at the later date a supplemental medwatch will be sent. Please provide the product code and the lot number of the product used, as already stated no further information is available.
Patient Sequence No: 1, Text Type: N, H10


[88073264] It was reported that a rodent underwent a test procedure on (b)(6) 2017 and the unknown suture was used. It was also reported that the unknown suture/wire easily broke. Additional information has been requested.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2210968-2017-70388
MDR Report Key6909188
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2017-10-02
Date of Report2017-09-04
Date of Event2017-09-04
Date Mfgr Received2017-09-04
Date Added to Maude2017-10-02
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 088760151
Manufacturer CountryUS
Manufacturer Postal088760151
Manufacturer Phone9082182792
Manufacturer G1ETHICON INC.
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUNKNOWN SUTURE
Generic NameSUTURE, NONABSORBABLE
Product CodeGAO
Date Received2017-10-02
Catalog NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerETHICON INC.
Manufacturer AddressP.O. BOX 151, ROUTE 22 WEST SOMERVILLE 088760151 US 088760151


Patients

Patient NumberTreatmentOutcomeDate
10 2017-10-02

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