MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 1999-01-20 for HEANEY HYSTERECTOMY FORCEPS GL3100 manufactured by Allegiance Healthcare Corp..
[154873]
Tip of the instrument fractured off inside of the pt during an abdominal hysterectomy. X-ray taken and the tip was retrieved from the pt without incident.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1423507-1999-00013 |
MDR Report Key | 206902 |
Report Source | 05,06 |
Date Received | 1999-01-20 |
Date of Report | 1999-01-19 |
Date of Event | 1998-12-17 |
Date Mfgr Received | 1999-01-07 |
Date Added to Maude | 1999-01-22 |
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 | 0 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HEANEY HYSTERECTOMY FORCEPS |
Generic Name | INSTRUMENT |
Product Code | HCZ |
Date Received | 1999-01-20 |
Returned To Mfg | 1999-01-14 |
Model Number | GL3100 |
Catalog Number | GL3100 |
Lot Number | UNK |
ID Number | NA |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 198703 |
Manufacturer | ALLEGIANCE HEALTHCARE CORP. |
Manufacturer Address | 1500 WAUKEGAN ROAD MCGAW PARK IL 60085 US |
Baseline Brand Name | HEANEY HYSTERECTOMY FORCEPS |
Baseline Generic Name | INSTRUMENT |
Baseline Model No | GL3100 |
Baseline Catalog No | GL3100 |
Baseline ID | NA |
Baseline Device Family | INSTRUMENT |
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 | 1999-01-20 |