MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-02-21 for HUDSON ET TUBE HOLDER, STANDARD 81801 manufactured by Teleflex Medical Sdn. Bhd..
[183744937]
(b)(4).
Patient Sequence No: 1, Text Type: N, H10
[183744938]
Customer reported the clip broke off device during use. The strap could not be adjusted and the provider had to cut off the device and start with a new one. Additional information was requested, but not available at the time of this report.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 8040412-2020-00056 |
| MDR Report Key | 9740821 |
| Report Source | COMPANY REPRESENTATIVE,USER F |
| Date Received | 2020-02-21 |
| Date of Report | 2020-02-05 |
| Date of Event | 2020-01-22 |
| Date Mfgr Received | 2020-03-26 |
| Date Added to Maude | 2020-02-21 |
| 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 | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | KATHARINE TARPLEY |
| Manufacturer Street | 3015 CARRINGTON MILL BLVD |
| Manufacturer City | MORRISVILLE NC 27560 |
| Manufacturer Country | US |
| Manufacturer Postal | 27560 |
| Manufacturer Phone | 9194334854 |
| Manufacturer G1 | TELEFLEX MEDICAL SDN. BHD. |
| Manufacturer Street | LOT NO : PT2577 JALEN PERUSAHAAN 4 KAMUNTING INDUSTRIAL ESTATE |
| Manufacturer City | PERAK, WEST MALAYSIA 34600 |
| Manufacturer Country | MY |
| Manufacturer Postal Code | 34600 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | HUDSON ET TUBE HOLDER, STANDARD |
| Generic Name | TRACHEAL TUBE FIXATION DEVICE |
| Product Code | CBH |
| Date Received | 2020-02-21 |
| Catalog Number | 81801 |
| Lot Number | 34913 |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | TELEFLEX MEDICAL SDN. BHD. |
| Manufacturer Address | PERAK, WEST MALAYSIA |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-02-21 |