MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 1996-10-22 for STABILIZED COLD KNIFE G-500 manufactured by Circon Acmi.
[15010689]
Cold knife blade broke during procedure; part of broken blade not found; x-ray and cystoscopy procedures failed to find missing piece.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1519132-1996-00015 |
MDR Report Key | 45118 |
Report Source | 06 |
Date Received | 1996-10-22 |
Date of Report | 1996-09-26 |
Date of Event | 1996-03-19 |
Device Manufacturer Date | 1987-08-01 |
Date Added to Maude | 1996-10-30 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Remedial Action | OT |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | STABILIZED COLD KNIFE |
Generic Name | COLD KNIFE |
Product Code | EZO |
Date Received | 1996-10-22 |
Returned To Mfg | 1996-09-26 |
Model Number | G-500 |
Catalog Number | G-500 |
Lot Number | * |
ID Number | * |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | * |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | * |
Device Sequence No | 1 |
Device Event Key | 46012 |
Manufacturer | CIRCON ACMI |
Manufacturer Address | 93 N PLEASANT ST NORWALK OH 448570409 US |
Baseline Brand Name | CLASSIC SERIES STABILIZED COLD KNIFE |
Baseline Generic Name | URETHROTOME |
Baseline Model No | G500 |
Baseline Catalog No | G500 |
Baseline ID | NA |
Baseline Device Family | COLD KNIFE |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | Y |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1996-10-22 |