MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2018-06-01 for VNGD SSK 360 FEMUR L 57.5 185281 manufactured by Zimmer Biomet, Inc..
[109749237]
(b)(4). Customer has indicated that the product is in process of being returned to zimmer biomet for investigation. Once the investigation has been completed, a follow-up mdr will be submitted. If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly. Zimmer biomet will continue to monitor for trends. H3 other text : product not returned
Patient Sequence No: 1, Text Type: N, H10
[109749238]
It was reported that the sterile packaging was found to be cracked at stock inspection.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 0001825034-2018-03738 |
MDR Report Key | 7559951 |
Report Source | COMPANY REPRESENTATIVE,DISTRI |
Date Received | 2018-06-01 |
Date of Report | 2018-10-15 |
Date of Event | 2018-05-02 |
Date Mfgr Received | 2018-10-03 |
Device Manufacturer Date | 2016-05-09 |
Date Added to Maude | 2018-06-01 |
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 |
Reporter Occupation | MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. CHRISTINA ARNT |
Manufacturer Street | 56 E. BELL DR. |
Manufacturer City | WARSAW IN 46582 |
Manufacturer Country | US |
Manufacturer Postal | 46582 |
Manufacturer Phone | 5745273773 |
Manufacturer G1 | ZIMMER BIOMET, INC. |
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 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | VNGD SSK 360 FEMUR L 57.5 |
Generic Name | KNEE, PROSTHESIS |
Product Code | MBV |
Date Received | 2018-06-01 |
Returned To Mfg | 2018-06-22 |
Catalog Number | 185281 |
Lot Number | 3779016 |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ZIMMER BIOMET, INC. |
Manufacturer Address | 56 E. BELL DRIVE WARSAW IN 46582 US 46582 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-06-01 |