MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1993-01-08 for PCA PRIMARY KNEE 6638-5-611 manufactured by Howmedica, Inc..
[1804]
Insert was worn through and needed to be replaced. Replaced insert and baseplatedevice labeled for single use. Patient medical status prior to event: unknown. There was not multiple patient involvement. Invalid data - on device service/maintenance. No data - regarding date last serviced. Service provided by: invalid data. Invalid data - service records availability. No imminent hazard to public health claimed. Invalid data - whether device used as labeled/intended. Device was not evaluated after the event. Method of evaluation: no data. Results of evaluation: no data. Conclusion: no data. Certainty of device as cause of or contributor to event: yes. Corrective actions: no data. Invalid data - on device destroyed/disposed of status.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 33446-1992-00012 |
| MDR Report Key | 2239 |
| Date Received | 1993-01-08 |
| Date of Report | 1992-12-08 |
| Date of Event | 1992-12-07 |
| Date Facility Aware | 1992-12-08 |
| Report Date | 1992-12-08 |
| Date Reported to FDA | 1992-12-08 |
| Date Reported to Mfgr | 1992-12-08 |
| Date Added to Maude | 1993-01-27 |
| 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 | 0 |
| Reporter Occupation | UNKNOWN |
| 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 | PCA PRIMARY KNEE |
| Generic Name | TOTAL KNEE |
| Product Code | MBD |
| Date Received | 1993-01-08 |
| Catalog Number | 6638-5-611 |
| Lot Number | UNKNOWN |
| Operator | OTHER HEALTH CARE PROFESSIONAL |
| Device Availability | * |
| Implant Flag | Y |
| Device Sequence No | 1 |
| Device Event Key | 2065 |
| Manufacturer | HOWMEDICA, INC. |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 1993-01-08 |