MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-20 for GLENOSPHERE - 36MM DIA X 6MM THK CONCENTRIC 5573-C-3606 manufactured by Stryker Gmbh.
Report Number | 0008031020-2020-00771 |
MDR Report Key | 9862305 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-03-20 |
Date of Report | 2020-03-20 |
Date of Event | 2019-12-20 |
Date Mfgr Received | 2020-02-26 |
Date Added to Maude | 2020-03-20 |
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 | MR. KEVIN SMITH |
Manufacturer Street | 325 CORPORATE DRIVE |
Manufacturer City | MAHWAH NJ 07430 |
Manufacturer Country | US |
Manufacturer Postal | 07430 |
Manufacturer Phone | 2018315000 |
Manufacturer G1 | STRYKER ORTHOPAEDICS-MAHWAH |
Manufacturer Street | 325 CORPORATE DRIVE |
Manufacturer City | MAHWAH NJ 07430 |
Manufacturer Country | US |
Manufacturer Postal Code | 07430 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | GLENOSPHERE - 36MM DIA X 6MM THK CONCENTRIC |
Generic Name | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED |
Product Code | KWS |
Date Received | 2020-03-20 |
Returned To Mfg | 2020-01-29 |
Model Number | 5573-C-3606 |
Catalog Number | 5573-C-3606 |
Lot Number | YT175R |
Operator | LAY USER/PATIENT |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | STRYKER GMBH |
Manufacturer Address | BOHNACKERWEG 1 POSTFACH SELZACH 2545 CH 2545 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-20 |