MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2019-06-14 for DR COMFORT GSA WINNER BLACK 11.5 XWIDE 5710-X-11.5 manufactured by Dr. Comfort, A Djo, Llc Company.
Report Number | 3008579854-2019-00007 |
MDR Report Key | 8699369 |
Report Source | USER FACILITY |
Date Received | 2019-06-14 |
Date of Report | 2019-06-13 |
Date of Event | 2019-05-28 |
Date Mfgr Received | 2019-05-28 |
Date Added to Maude | 2019-06-14 |
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. BRIAN BECKER |
Manufacturer Street | 2900 LAKE VISTA DRIVE |
Manufacturer City | LEWISVILLE TX 75067 |
Manufacturer Country | US |
Manufacturer Postal | 75067 |
Manufacturer G1 | DR. COMFORT, A DJO, LLC COMPANY |
Manufacturer Street | 10300 ENTERPRISE DR. |
Manufacturer City | MEQUON, WI 53092 |
Manufacturer Country | US |
Manufacturer Postal Code | 53092 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DR COMFORT GSA WINNER BLACK 11.5 XWIDE |
Generic Name | ORTHOSIS, CORRECTIVE SHOE |
Product Code | KNP |
Date Received | 2019-06-14 |
Model Number | 5710-X-11.5 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DR. COMFORT, A DJO, LLC COMPANY |
Manufacturer Address | 10300 ENTERPRISE DR. MEQUON, WI 53092 US 53092 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-06-14 |