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 2020-02-11 for HUDSON ET TUBE HOLDER, STANDARD 81801 manufactured by Teleflex Medical Sdn. Bhd..
[183743193]
(b)(4).
Patient Sequence No: 1, Text Type: N, H10
[183743194]
Customer reported the respiratory therapist was unable to loosen the clamp to release the ett. The respiratory therapist used a blade to cut the securement loop to allow the tube to be manipulated. The device was replaced. No patient or provider harm reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 8040412-2020-00040 |
MDR Report Key | 9693715 |
Report Source | COMPANY REPRESENTATIVE,USER F |
Date Received | 2020-02-11 |
Date of Report | 2020-01-22 |
Date of Event | 2020-01-21 |
Date Mfgr Received | 2020-03-27 |
Date Added to Maude | 2020-02-11 |
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 | 2020-02-11 |
Returned To Mfg | 2020-02-04 |
Catalog Number | 81801 |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
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 | 2020-02-11 |