MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2006-06-14 for WINER GRASPING FORCEPS, IN-LINE, RATCHET, 5MM, 33CM * 600-123 manufactured by Tontarra Medizintechnik Gmbh.
[488464]
User facility reported the jaw of the instrument locked in place and broke during a surgical procedure to remove a pt's gall bladder from the liver. No pt injury has been reported.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2430952-2006-00027 |
| MDR Report Key | 727405 |
| Date Received | 2006-06-14 |
| Date of Report | 2006-06-14 |
| Date Facility Aware | 2006-05-15 |
| Report Date | 2006-06-14 |
| Date Added to Maude | 2006-06-22 |
| Event Key | 0 |
| Report Source Code | Distributor report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | WINER GRASPING FORCEPS, IN-LINE, RATCHET, 5MM, 33CM |
| Generic Name | JARIT ENDOSCOPIC INST. |
| Product Code | EMH |
| Date Received | 2006-06-14 |
| Model Number | * |
| Catalog Number | 600-123 |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 715805 |
| Manufacturer | TONTARRA MEDIZINTECHNIK GMBH |
| Manufacturer Address | * WURMLINGEN GM |
| Baseline Brand Name | WINER GRASPING FORCEPS, IN LINE RATCHET 5MM 33CM |
| Baseline Generic Name | JARIT ENDOSCOPIC INSTRUMENTS |
| Baseline Model No | * |
| Baseline Catalog No | 600-123 |
| Baseline ID | * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2006-06-14 |