MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06 report with the FDA on 2012-09-07 for DOBBHOFF FEEDING TUBE 8884711253 manufactured by Covidien.
[3115167]
It was reported to covidien on (b)(6) 2012 that a customer had an issue with a feeding tube. The customer reports that during the removal of the tube, it broke and a part stayed inside the patient. The part had to be removed by endoscopy. No patient injury reported.
Patient Sequence No: 1, Text Type: D, B5
[10184312]
Submit date: (b)(4) 2012. An investigation is currently underway, upon completion, the results will be forwarded.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 9612030-2012-00048 |
| MDR Report Key | 2745108 |
| Report Source | 01,05,06 |
| Date Received | 2012-09-07 |
| Date of Report | 2012-08-16 |
| Report Date | 2012-08-16 |
| Date Reported to Mfgr | 2012-08-16 |
| Date Mfgr Received | 2012-08-16 |
| Date Added to Maude | 2012-09-18 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| 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 | 3 |
| Report to FDA | 0 |
| Event Location | 3 |
| Manufacturer Contact | KARLA CALDERON |
| Manufacturer Street | 15 HAMPSHIRE STREET |
| Manufacturer City | MANSFIELD MA 02048 |
| Manufacturer Country | US |
| Manufacturer Postal | 02048 |
| Manufacturer Phone | 5082618622 |
| Manufacturer G1 | COVIDIEN |
| Manufacturer Street | CALLE 9 SUR NO. 125 CUIDAD INDUSTRIAL |
| Manufacturer City | TIJUANA 92173 |
| Manufacturer Country | MX |
| Manufacturer Postal Code | 92173 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DOBBHOFF FEEDING TUBE |
| Generic Name | FEEDING TUBE |
| Product Code | FDP |
| Date Received | 2012-09-07 |
| Model Number | 8884711253 |
| Catalog Number | 8884711253 |
| Lot Number | G1034429 |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | NA |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COVIDIEN |
| Manufacturer Address | CALLE 9 SUR NO. 125 TIJUANA 92173 MX 92173 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2012-09-07 |