MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 1998-07-08 for CIRCON ACMI DISPOSABLE ACTIVE CORD DAC manufactured by Circon Acmi.
[20934001]
Sparking and smoking reportedly observed at connection between cautery cord and resectoscope.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1519132-1998-00049 |
MDR Report Key | 176572 |
Report Source | 06 |
Date Received | 1998-07-08 |
Date of Report | 1998-07-08 |
Date of Event | 1998-06-01 |
Date Mfgr Received | 1998-06-10 |
Device Manufacturer Date | 1997-05-01 |
Date Added to Maude | 1998-07-14 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 0 |
Reprocessed and Reused Flag | 0 |
Health Professional | 0 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Single Use | 3 |
Remedial Action | RP |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CIRCON ACMI DISPOSABLE ACTIVE CORD |
Generic Name | ACTIVE CORD |
Product Code | FFZ |
Date Received | 1998-07-08 |
Returned To Mfg | 1998-06-10 |
Model Number | DAC |
Catalog Number | DAC |
Lot Number | EA (5/97) |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 166897 |
Manufacturer | CIRCON ACMI |
Manufacturer Address | 93 NORTH PLEASANT STREET NORWALK OH 448570409 US |
Baseline Brand Name | DISPOSABLE ACTIVE CORD |
Baseline Generic Name | ACTIVE CORD |
Baseline Model No | DAC |
Baseline Catalog No | DAC |
Baseline ID | NA |
Baseline Device Family | ACTIVE CORD |
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 | 1998-07-08 |