MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1994-11-30 for TRITON TREATMENT TABLE TRE-DH5 manufactured by Chattanooga Group.
[20897192]
When the plastic shaft of the hand switch which holds the switch in position breaks, the switch stays in the on position. The switch broke while a pt was on the table. The pt was removed but the table had to be unplugged to stop it from going down. The table has been in use for two yrs; this was the second time the hand switch had broken.
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW1004220 |
MDR Report Key | 18059 |
Date Received | 1994-11-30 |
Date of Report | 1994-11-28 |
Date Added to Maude | 1994-12-01 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Reporter Occupation | RISK MANAGER |
Health Professional | 3 |
Initial Report to FDA | 0 |
Report to FDA | 0 |
Event Location | 3 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | TRITON TREATMENT TABLE |
Product Code | INW |
Date Received | 1994-11-30 |
Model Number | TRE-DH5 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Implant Flag | N |
Date Removed | B |
Device Sequence No | 1 |
Device Event Key | 17987 |
Manufacturer | CHATTANOOGA GROUP |
Manufacturer Address | HIXSON TN 37342 US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1994-11-30 |