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.
[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
Report Number | 7583 |
MDR Report Key | 7583 |
Date Received | 1994-01-17 |
Date of Report | 1993-07-15 |
Date of Event | 1993-07-09 |
Date Facility Aware | 1993-07-09 |
Report Date | 1993-07-15 |
Date Reported to Mfgr | 1993-07-15 |
Date Added to Maude | 1994-05-02 |
Event Key | 0 |
Report Source Code | User Facility report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 0 |
Initial Report to FDA | 0 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PDS SUTURE |
Product Code | HAS |
Date Received | 1994-01-17 |
Model Number | PDS II VIOLET MONEFILAMENT |
Catalog Number | 2-0 27" |
Operator | OTHER HEALTH CARE PROFESSIONAL |
Device Availability | Y |
Implant Flag | N |
Device Sequence No | 1 |
Device Event Key | 7262 |
Manufacturer | ETHICON |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 1994-01-17 |