MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-02-20 for ANATOMICAL SHOULDER REVERSE, SCREW SYSTEM, 4.5-30 N/A 01.04223.030 manufactured by Zimmer Gmbh.
Report Number | 0009613350-2020-00076 |
MDR Report Key | 9731864 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2020-02-20 |
Date of Report | 2020-02-20 |
Date of Event | 2020-01-17 |
Date Mfgr Received | 2020-02-04 |
Device Manufacturer Date | 2017-10-24 |
Date Added to Maude | 2020-02-20 |
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. 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 GMBH |
Manufacturer Street | SULZER ALLEE 8 SULZER INDUSTRIE PARK |
Manufacturer City | WINTERTHUR 8404 |
Manufacturer Country | SZ |
Manufacturer Postal Code | 8404 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | N/A |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ANATOMICAL SHOULDER REVERSE, SCREW SYSTEM, 4.5-30 |
Generic Name | ZIMMER TRABECULAR METAL REVERSE SHOULDER SYSTEM |
Product Code | KWT |
Date Received | 2020-02-20 |
Model Number | N/A |
Catalog Number | 01.04223.030 |
Lot Number | 2913097 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ZIMMER GMBH |
Manufacturer Address | SULZER ALLEE 8 SULZER INDUSTRIE PARK WINTERTHUR 8404 SZ 8404 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2020-02-20 |