MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2015-05-06 for DONJOY OA ADJUSTER 3, MEDIAL, RT, S 11-1590-2 manufactured by Djo, Llc.
[21123714]
Complaint received from clinician that alleges "bent when he fell- and having ankle problems was not able to feel his foot as a result of the fall". Questionnaire was not received from clinician and/or patient. Device not returned to manufacturer for evaluation. No indication event caused or contributed to permanent impairment or death. No indication device caused or contributed to the event.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9616086-2015-00011 |
| MDR Report Key | 4758516 |
| Report Source | 05 |
| Date Received | 2015-05-06 |
| Date of Report | 2015-05-06 |
| Date of Event | 2015-04-20 |
| Date Added to Maude | 2015-05-11 |
| 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 | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Street | 1430 DECISION STREET |
| Manufacturer City | VISTA CA 92081 |
| Manufacturer Country | US |
| Manufacturer Postal | 92081 |
| Manufacturer Phone | 7607271280 |
| Manufacturer G1 | DJ ORTHOPEDICS DE MEXICO, S.A. DE C.V. |
| Manufacturer Street | CARRETERA LIBRE TIJUANA TECATE 20230 SUBMETROPOLI EL FLORIDO |
| Manufacturer City | TIJUANA 22244 |
| Manufacturer Country | MX |
| Manufacturer Postal Code | 22244 |
| Single Use | 0 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DONJOY OA ADJUSTER 3, MEDIAL, RT, S |
| Generic Name | OA ADJUSTER 3, MEDIAL, RT, S KNEE BRACE |
| Product Code | ITM |
| Date Received | 2015-05-06 |
| Model Number | 11-1590-2 |
| Catalog Number | 11-1590-2 |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| 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. Other | 2015-05-06 |