MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 99 report with the FDA on 2013-04-01 for CHATTANOOGA HYDROCOLLATOR manufactured by Djo, Llc.
[3412482]
"received court documents stating that the plaintiff was electrocuted by a hydrocollator while attempting to unplug the product from an electrical outlet. " initial notification of complaint was a copy of court document notification of civil action. No additional info supplied to us for eval. Product not returned to us for eval.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9616086-2013-00002 |
MDR Report Key | 3032496 |
Report Source | 99 |
Date Received | 2013-04-01 |
Date of Report | 2013-04-01 |
Date of Event | 2011-08-22 |
Date Mfgr Received | 2013-03-04 |
Date Added to Maude | 2013-04-04 |
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 ST. |
Manufacturer City | VISTA CA 92081 |
Manufacturer Country | US |
Manufacturer Postal | 92081 |
Manufacturer G1 | DJ ORTHOPEDICS DE MEXICO, S.A. DE C.V. |
Manufacturer Street | 20230 SUBMETROPOLI EL FLORIDO CARRETERA LIBRE TIJUANA TECATE |
Manufacturer City | TIJUANA 22244 |
Manufacturer Country | MX |
Manufacturer Postal Code | 22244 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CHATTANOOGA HYDROCOLLATOR |
Generic Name | HYDROCOLLATOR |
Product Code | IMA |
Date Received | 2013-04-01 |
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 92081 US 92081 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2013-04-01 |