MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-05-30 for BARD NG SUMP TUBE manufactured by C. R. Bard, Inc..
[146924106]
Ng tube placed but unable to auscultate correct placement. Removed and replaced by a different nurse, still unable to auscultate placement verification. Placed 5 cc's water in syringe to flush ng tube, water came out of blue pigtail. New ng tube obtained and inserted without difficulty. Auscultation of air bolus was heard. Fda safety report id# (b)(4).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5087042 |
| MDR Report Key | 8658582 |
| Date Received | 2019-05-30 |
| Date of Report | 2019-05-29 |
| Date of Event | 2019-03-14 |
| Date Added to Maude | 2019-05-31 |
| 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 | BARD NG SUMP TUBE |
| Generic Name | TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND / OR INTUBATION |
| Product Code | FEG |
| Date Received | 2019-05-30 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | C. R. BARD, INC. |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2019-05-30 |