MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,other report with the FDA on 2019-02-28 for ALTRX +4 NEUT 36IDX52OD 122136452 manufactured by Depuy Orthopaedics Inc Us.
[137408357]
If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate. Device was used for treatment, not diagnosis.
Patient Sequence No: 1, Text Type: N, H10
[137408358]
Ppf and sticker sheets record received. Pinnacle ppf alleges infection and dislocation after first revision. Doi: (b)(6) 2010 - dor: none reported, (left hip).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1818910-2019-86021 |
| MDR Report Key | 8378108 |
| Report Source | CONSUMER,OTHER |
| Date Received | 2019-02-28 |
| Date of Report | 2019-02-08 |
| Date Mfgr Received | 2019-03-11 |
| Device Manufacturer Date | 2010-02-09 |
| Date Added to Maude | 2019-02-28 |
| 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 | MS. KARA DITTY-BOVARD |
| Manufacturer Street | 1210 WARD AVENUE |
| Manufacturer City | WEST CHESTER IN 193800988 |
| Manufacturer Country | US |
| Manufacturer Postal | 193800988 |
| Manufacturer Phone | 6103142063 |
| Manufacturer G1 | DEPUY ORTHOPAEDICS INC US |
| Manufacturer Street | 700 ORTHOPAEDIC DRIVE |
| Manufacturer City | WARSAW IN 465820988 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 465820988 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ALTRX +4 NEUT 36IDX52OD |
| Generic Name | PINNACLE HIP SYSTEM : HIP POLY ACETABULAR LINERS |
| Product Code | LPH |
| Date Received | 2019-02-28 |
| Catalog Number | 122136452 |
| Lot Number | EE4M31000 |
| Device Expiration Date | 2015-02-28 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | DEPUY ORTHOPAEDICS INC US |
| Manufacturer Address | 700 ORTHOPAEDIC DRIVE WARSAW IN 465820988 US 465820988 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2019-02-28 |