MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2015-08-05 for UNKNOWN NEXGEN TIBIA manufactured by Zimmer, Inc..
[22500945]
This report will be amended when our investigation is complete.
Patient Sequence No: 1, Text Type: N, H10
[22500946]
It is reported that the patient is experiencing pain.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1822565-2015-01411 |
| MDR Report Key | 4987841 |
| Report Source | COMPANY REPRESENTATIVE,CONSUM |
| Date Received | 2015-08-05 |
| Date of Report | 2015-07-07 |
| Date Mfgr Received | 2015-07-07 |
| Date Added to Maude | 2015-08-10 |
| 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 | 3 |
| Event Location | 3 |
| Manufacturer Contact | KEVIN ESCAPULE |
| Manufacturer Street | PO BOX 708 |
| Manufacturer City | WARSAW IN 46580 |
| Manufacturer Country | US |
| Manufacturer Postal | 46580 |
| Manufacturer Phone | 8006316131 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | UNKNOWN NEXGEN TIBIA |
| Generic Name | KNEE PROSTHESIS |
| Product Code | HSH |
| Date Received | 2015-08-05 |
| Operator | HEALTH PROFESSIONAL |
| 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 | PO BOX 708 WARSAW IN 46580 US 46580 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2015-08-05 |