MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 02,05,07 report with the FDA on 2009-04-09 for ZIMMER SEGMENTAL SYSTEM ARTICULAR SURFACE WITH SEGMENTAL HINGE POST 00585004014 manufactured by Zimmer, Inc..
[19938848]
Evaluation summary: no product was returned for evaluation. Also, no x-rays were returned for review. Patient information such as height, weight and patient activity is unknown. Based on the available information, a definitive cause cannot be determined. No product was returned. Review of the device history records was also not possible, as the product and/or lot numbers required for retrieval were unavailable. It is not suspected that the product failed to meet specifications. The investigation could not verify or identify any evidence of product contribution to the reported problem. Based on the available information, the need for corrective action is not indicated. Should additional substantive information be received, the complaint will be reopened. Zimmer, inc. Considers the investigation closed.
Patient Sequence No: 1, Text Type: N, H10
[20024477]
It is reported that the device was implanted in 2009, and that the patient was revised four days later, due to a hematoma.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1822565-2009-00417 |
| MDR Report Key | 1359395 |
| Report Source | 02,05,07 |
| Date Received | 2009-04-09 |
| Date of Report | 2009-03-13 |
| Date of Event | 2009-02-18 |
| Date Mfgr Received | 2009-03-13 |
| Date Added to Maude | 2009-04-16 |
| 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 | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Contact | BRIAN FIEDLER |
| Manufacturer Street | P.O. BOX 708 |
| Manufacturer City | WARSAW IN 465810708 |
| Manufacturer Country | US |
| Manufacturer Postal | 465810708 |
| Manufacturer Phone | 8006136131 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ZIMMER SEGMENTAL SYSTEM ARTICULAR SURFACE WITH SEGMENTAL HINGE POST |
| Generic Name | KNEE PROSTHESIS |
| Product Code | HRZ |
| Date Received | 2009-04-09 |
| Model Number | NA |
| Catalog Number | 00585004014 |
| Lot Number | UNK |
| ID Number | NA |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ZIMMER, INC. |
| Manufacturer Address | P.O. BOX 708 WARSAW IN 46581070 US 46581 0708 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2009-04-09 |