MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2010-10-21 for HUDSON BITE-GARD 1140 manufactured by Teleflex Medical.
[1688474]
The event is reported as: the green piece of the bite-gard became detached from the white arm. The alleged incident occurred on a pt during an unspecified med procedure. The complaint indicates that the pt was very combative and the med staff had problems sedating the pt. No pt injury reported.
Patient Sequence No: 1, Text Type: D, B5
[8896573]
The results of the investigation are not available at the time of this report.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 3004365956-2010-00320 |
MDR Report Key | 1889182 |
Report Source | 05,06,07 |
Date Received | 2010-10-21 |
Date of Report | 2010-10-05 |
Date of Event | 2010-10-05 |
Date Mfgr Received | 2010-10-05 |
Date Added to Maude | 2011-02-11 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | MICHAEL TAGGART, VP |
Manufacturer Street | P.O. BOX 12600 |
Manufacturer City | RTP NC 27709 |
Manufacturer Country | US |
Manufacturer Postal | 27709 |
Manufacturer Phone | 9194334916 |
Manufacturer G1 | TELEFLEX MEDICAL |
Manufacturer Street | AVE TRANSFORMACION 5954 PARQUE INDUSTRIAL FINSA |
Manufacturer City | NUEVO LAREDO 88275 |
Manufacturer Country | MX |
Manufacturer Postal Code | 88275 |
Single Use | 3 |
Remedial Action | OT |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HUDSON BITE-GARD |
Generic Name | BITE BLOCKS |
Product Code | JXL |
Date Received | 2010-10-21 |
Model Number | NA |
Catalog Number | 1140 |
Lot Number | 02F0900762 |
ID Number | NA |
Operator | OTHER |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TELEFLEX MEDICAL |
Manufacturer Address | NUEVO LAREDO MX |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2010-10-21 |