MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2008-10-20 for COMPAX 40E manufactured by Ge Medical Systems, Llc.
[18906632]
The ge field engineer (fe) found a blown 2-amp fuse. When the fe replaced the fuse, it was verified that the locks were performing according to specs.
Patient Sequence No: 1, Text Type: N, H10
[18914477]
It was reported that the table locks did not actuate, causing the tabletop to unexpectedly move in both the longitudinal and lateral directions without resistance (free float). The problem was discovered as the operator was positioning the pt. There was no report of a fall or injury. This situation could contribute to an injury if a pt or operator were unaware of this condition while loading or unloading a pt. The ensuing instability could lead to a fall.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2126677-2008-00085 |
| MDR Report Key | 1204588 |
| Report Source | 05 |
| Date Received | 2008-10-20 |
| Date of Report | 2008-08-16 |
| Date of Event | 2008-08-16 |
| Date Mfgr Received | 2008-08-16 |
| Device Manufacturer Date | 1999-11-01 |
| Date Added to Maude | 2009-08-20 |
| 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 | MARTHA KAMROW |
| Manufacturer Street | 3000 N GRANDVIEW BLVD. |
| Manufacturer City | WAUKESHA WI 53188 |
| Manufacturer Country | US |
| Manufacturer Postal | 53188 |
| Manufacturer Phone | 2623127196 |
| Manufacturer G1 | GE MEDICAL SYSTEMS, LLC |
| Manufacturer Street | 3000 N GRANDVIEW BLVD. |
| Manufacturer City | WAUKESHA WI 53188 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 53188 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | COMPAX 40E |
| Product Code | IZZ |
| Date Received | 2008-10-20 |
| ID Number | SYSTEMID SA1001RX1 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | GE MEDICAL SYSTEMS, LLC |
| Manufacturer Address | 3000 N GRANDVIEW BLVD. WAUKESHA WI 53188 US 53188 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2008-10-20 |