MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1994-11-10 for CLAY ADAMS 20034-112 manufactured by Becton Dickinson And Co..
[11824]
Cantor tube removed from pt without mercury.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1003978 |
| MDR Report Key | 17562 |
| Date Received | 1994-11-10 |
| Date of Report | 1994-10-20 |
| Date of Event | 1994-10-19 |
| Date Added to Maude | 1994-11-14 |
| 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 |
| 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 | CLAY ADAMS |
| Generic Name | CANTOR TUBE |
| Product Code | FEF |
| Date Received | 1994-11-10 |
| Catalog Number | 20034-112 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 17483 |
| Manufacturer | BECTON DICKINSON AND CO. |
| Manufacturer Address | FRANKLIN LAKES NJ 07417 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 1994-11-10 |