MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2015-08-20 for G7 CURVED ACET SHELL INSERTER N/A 110003453 manufactured by Biomet Orthopedics.
[23598164]
Current information is insufficient to permit a conclusion as to the cause of the event.
Patient Sequence No: 1, Text Type: N, H10
[23598165]
It was reported that a surgeon has experienced fracture of the impactor when medializing the acetabular cup during total hip arthroplasty procedures. There has been no reported injuries to patients as a result. Follow up attempts to obtain additional information have been made; however, there is no additional information available.
Patient Sequence No: 1, Text Type: D, B5
[26562199]
This follow-up report is being filed to relay additional information, which was unknown at the time of the initial medwatch.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 0001825034-2015-03683 |
MDR Report Key | 5018589 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2015-08-20 |
Date of Report | 2015-09-04 |
Date Mfgr Received | 2015-09-04 |
Date Added to Maude | 2015-08-20 |
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. MEGAN HAAS |
Manufacturer Street | 56 E. BELL DRIVE |
Manufacturer City | WARSAW IN 46582 |
Manufacturer Country | US |
Manufacturer Postal | 46582 |
Manufacturer Phone | 5743726700 |
Manufacturer G1 | BIOMET ORTHOPEDICS |
Manufacturer Street | 56 E. BELL DRIVE |
Manufacturer City | WARSAW IN 46582 |
Manufacturer Country | US |
Manufacturer Postal Code | 46582 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | N/A |
Event Type | 3 |
Type of Report | 3 |
Brand Name | G7 CURVED ACET SHELL INSERTER |
Generic Name | PROSTHESIS, HIP |
Product Code | LKD |
Date Received | 2015-08-20 |
Model Number | N/A |
Catalog Number | 110003453 |
Lot Number | UNKNOWN |
ID Number | N/A |
Operator | PHYSICIAN |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BIOMET ORTHOPEDICS |
Manufacturer Address | 56 E. BELL DRIVE WARSAW IN 46582 US 46582 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2015-08-20 |