MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-12 for BARD NASOGASTRIC SUMP NG TUBE manufactured by C.r. Bard, Inc..
[136873461]
Ng tubes do not have adequate measurement markings. Markings are limited to 18'', 22", 26", and 30. " staff are unable to mark proper placement and are unable to identify when "the ng tubes move in the patient. Dislodgement may go unnoticed due to lack of markings.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5084017 |
| MDR Report Key | 8336992 |
| Date Received | 2019-02-12 |
| Date of Report | 2019-02-11 |
| Date of Event | 2019-01-23 |
| Date Added to Maude | 2019-02-13 |
| 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 NASOGASTRIC SUMP NG TUBE |
| Generic Name | TUBE, NASOGASTRIC |
| Product Code | BSS |
| Date Received | 2019-02-12 |
| Lot Number | NGCX0244 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | C.R. BARD, INC. |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-02-12 |