MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2020-02-11 for DONJOY DEFIANCE III CONV DEFIANCE III manufactured by Djo, Llc.
[182180357]
No device was returned for evaluation. If the device is received, a follow-up report will be submitted upon completion of product evaluation.
Patient Sequence No: 1, Text Type: N, H10
[182180358]
It was reported that the patient "lost my balance and did one or two cartwheels and pop. I'm guessing my knee was hyperextended as i was cartwheeling and as the ski popped off so did my acl (anterior cruciate ligament). I waited a couple minutes to let the pain subside but the second i tried to click back into my ski i knew the acl was gone. I skied down on my left ski to the door of the first aid clinic at the base of the resort. " no further information is currently available.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3012446970-2020-00004 |
MDR Report Key | 9694714 |
Report Source | CONSUMER |
Date Received | 2020-02-11 |
Date of Report | 2020-02-16 |
Date of Event | 2020-01-10 |
Date Mfgr Received | 2020-01-28 |
Device Manufacturer Date | 2012-02-24 |
Date Added to Maude | 2020-02-11 |
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 | 0 |
Initial Report to FDA | 0 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | BRIAN BECKER |
Manufacturer Street | 2900 LAKE VISTA DRIVE |
Manufacturer City | LEWISVILLE, TX |
Manufacturer Country | US |
Manufacturer G1 | DJO, LLC |
Manufacturer Street | 3151 SCOTT ST. |
Manufacturer City | VISTA, CA |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DONJOY DEFIANCE III |
Generic Name | JOINT, KNEE, EXTERNAL BRACE |
Product Code | ITQ |
Date Received | 2020-02-11 |
Returned To Mfg | 2020-02-14 |
Model Number | CONV DEFIANCE III |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DJO, LLC |
Manufacturer Address | 1430 DECISION STREET VISTA, CA US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-02-11 |