MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1994-03-21 for CANTOR TUBE 2330-16 manufactured by Rusch, Inc..
[22078096]
Cantor tube eroded or opened while in place in pt; mercury leaked into pt's bowels. No injury.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1001166 |
| MDR Report Key | 12145 |
| Date Received | 1994-03-21 |
| Date of Report | 1994-03-02 |
| Date of Event | 1994-02-01 |
| Date Added to Maude | 1994-03-22 |
| 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 | CANTOR TUBE |
| Generic Name | CANTOR TUBE |
| Product Code | FEF |
| Date Received | 1994-03-21 |
| Catalog Number | 2330-16 |
| Lot Number | E311203 |
| Device Availability | R |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 12145 |
| Manufacturer | RUSCH, INC. |
| Manufacturer Address | DULUTH GA 30136 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1994-03-21 |