MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 1998-02-26 for LERICHE HEOMSTATIC FORCEPS, DELICATE CH7000 manufactured by Allegiance Healthcare Corp..
[106954]
One side of the jaws on the hemostatic forceps fractured off when the surgeon clampled onto a suture.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1423507-1998-00057 |
MDR Report Key | 152933 |
Report Source | 05,06 |
Date Received | 1998-02-26 |
Date of Report | 1998-02-26 |
Date Mfgr Received | 1998-01-31 |
Device Manufacturer Date | 1997-01-01 |
Date Added to Maude | 1998-03-02 |
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 | LERICHE HEOMSTATIC FORCEPS, DELICATE |
Generic Name | INSTRUMENT |
Product Code | HRQ |
Date Received | 1998-02-26 |
Returned To Mfg | 1998-02-21 |
Model Number | CH7000 |
Catalog Number | CH7000 |
Lot Number | N |
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 | 148995 |
Manufacturer | ALLEGIANCE HEALTHCARE CORP. |
Manufacturer Address | 1500 WAUKEGAN RD. MCGAW PARK IL 60085 US |
Baseline Brand Name | LERICHE HEMOSTATIC FORCEPS, DEL |
Baseline Generic Name | HEMOSTATIC FORCEPS |
Baseline Model No | CH7000 |
Baseline Catalog No | CH7000 |
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 | 1. Other | 1998-02-26 |