PDS SUTURE PDS II VIOLET MONEFILAMENT 2-0 27"

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1994-01-17 for PDS SUTURE PDS II VIOLET MONEFILAMENT 2-0 27" manufactured by Ethicon.

Event Text Entries

[20474740] Suture broke away from needle, c-aim needle to find needle. Device labeled for single use. Patient medical status prior to event: unknown. There was not multiple patient involvement. Invalid data - on device service/maintenance. No data - regarding date last serviced. Service provided by: invalid data. Invalid data - service records availability. No imminent hazard to public health claimed. Device used as labeled/intended. Device was not evaluated after the event. Method of evaluation: no data. Results of evaluation: no data. Conclusion: no data. Certainty of device as cause of or contributor to event: yes. Corrective actions: no data. Invalid data - on device destroyed/disposed of status.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number7583
MDR Report Key7583
Date Received1994-01-17
Date of Report1993-07-15
Date of Event1993-07-09
Date Facility Aware1993-07-09
Report Date1993-07-15
Date Reported to Mfgr1993-07-15
Date Added to Maude1994-05-02
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NamePDS SUTURE
Product CodeHAS
Date Received1994-01-17
Model NumberPDS II VIOLET MONEFILAMENT
Catalog Number2-0 27"
OperatorOTHER HEALTH CARE PROFESSIONAL
Device AvailabilityY
Implant FlagN
Device Sequence No1
Device Event Key7262
ManufacturerETHICON


Patients

Patient NumberTreatmentOutcomeDate
101. Other 1994-01-17

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