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 2018-07-24 for AIRCAST 01EP-L manufactured by Djo, Llc.
[114845693]
Complaint received that alleges "after short time of wearing the walker wounds the patients foot".
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9616086-2018-00018 |
MDR Report Key | 7714381 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2018-07-24 |
Date of Report | 2018-12-19 |
Date of Event | 2018-07-12 |
Date Mfgr Received | 2018-07-12 |
Date Added to Maude | 2018-07-24 |
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 | BRIAN BECKER |
Manufacturer Street | 1430 DECISION ST |
Manufacturer City | VISTA CA 920819663 |
Manufacturer Country | US |
Manufacturer Postal | 920819663 |
Manufacturer Phone | 7607343126 |
Manufacturer G1 | DJO, LLC |
Manufacturer Street | 1430 DECISION ST 20230 SUBMETROPOLI EL FLORIDO |
Manufacturer City | VISTA CA 920819663 |
Manufacturer Country | US |
Manufacturer Postal Code | 920819663 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | AIRCAST |
Generic Name | AIRSELECT, ELITE, LARGE |
Product Code | ITW |
Date Received | 2018-07-24 |
Model Number | 01EP-L |
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 ST VISTA CA 920819663 US 920819663 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2018-07-24 |