MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-11-07 for DOBHOFF manufactured by Unk.
[91332169]
On (b)(6) 2017 as dobhoff tube removed, md, rn and pt heard pop and dobhoff tube removed and did not have weighted tip present on end of tube. Abd xray showed no tip. On (b)(6) 2017 sinus xray showed tip in r nare. Ent consulted and removed at bedside.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5073166 |
| MDR Report Key | 7006596 |
| Date Received | 2017-11-07 |
| Date of Report | 2017-11-03 |
| Date of Event | 2017-10-14 |
| Date Added to Maude | 2017-11-07 |
| 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 | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | DOBHOFF |
| Generic Name | NASALGASTRIC TUBE |
| Product Code | BSS |
| Date Received | 2017-11-07 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | UNK |
| Manufacturer Address | UNK UNK |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2017-11-07 |