MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 2012-01-24 for RUSCH GREENSPEC FO HANDLE MEDIUM 004411100 manufactured by Teleflex Medical.
[2422435]
The event is reported as: complaint alleges: customer called saying after handles were sterilized, batteries put in, then handle overheated and was too hot to touch. No pt injury reported.
Patient Sequence No: 1, Text Type: D, B5
[9589840]
The device sample was not received by the mfr at the time of this report. A f/u report will be sent when completion of investigation.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 3004365956-2012-00025 |
| MDR Report Key | 2442287 |
| Report Source | 06,07 |
| Date Received | 2012-01-24 |
| Date of Report | 2012-01-11 |
| Date of Event | 2012-01-11 |
| Date Mfgr Received | 2012-01-11 |
| Date Added to Maude | 2012-04-13 |
| 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 | 0 |
| Event Location | 0 |
| Manufacturer Contact | JASMINE BROWN |
| Manufacturer Street | PO BOX 12600 |
| Manufacturer City | DURHAM NC 27709 |
| Manufacturer Country | US |
| Manufacturer Postal | 27709 |
| Manufacturer Phone | 9193614124 |
| Manufacturer G1 | TELEFLEX |
| Manufacturer Street | AVE. TRANSFORMACION 5954 PARQUE INDUSTRIAL FINSA |
| Manufacturer City | NUEVO LAREDO 88275 |
| Manufacturer Country | MX |
| Manufacturer Postal Code | 88275 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | RUSCH GREENSPEC FO HANDLE MEDIUM |
| Generic Name | LARYNGOSCOPE HANDLE |
| Product Code | EQN |
| Date Received | 2012-01-24 |
| Catalog Number | 004411100 |
| Lot Number | UNK |
| Operator | OTHER |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | TELEFLEX MEDICAL |
| Manufacturer Address | NUEVO LAREDO MX |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2012-01-24 |