MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 1999-09-15 for USE ELITE/USA SERIES DISPOSABLE ACTIVE CORD DAC manufactured by Circon Acmi.
[19496072]
User facility reported that sparking occurred while using device. There was no patient injury.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1519132-1999-00069 |
MDR Report Key | 241333 |
Report Source | 06,07 |
Date Received | 1999-09-15 |
Date of Report | 1999-09-15 |
Date Mfgr Received | 1999-08-20 |
Device Manufacturer Date | 1999-02-01 |
Date Added to Maude | 1999-09-23 |
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 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | USE ELITE/USA SERIES DISPOSABLE ACTIVE CORD |
Generic Name | ACTIVE CORD |
Product Code | FFZ |
Date Received | 1999-09-15 |
Returned To Mfg | 1999-08-20 |
Model Number | DAC |
Catalog Number | DAC |
Lot Number | BC (2/99) |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 233819 |
Manufacturer | CIRCON ACMI |
Manufacturer Address | 93 NORTH PLEASANT ST. 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 | 1999-09-15 |