MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-03-27 for MELKER EMERGENCY CUFFED CRICOTHYROTOMY CATHETER SET G29432 C-TCCSB-500 manufactured by Cook Inc.
[103823703]
This mdr is being filed after the associated complaint was reviewed under remediation protocol cap(b)(6), complaint/mdr retrospective review and remediation and reassessed as reportable. Additional complaint investigation and record remediation was not performed.
Patient Sequence No: 1, Text Type: N, H10
[103823706]
It was reported that while the melker emergency cuffed cricothyrotomy catheter set was being used, the plastic part of the catheter introducer needle kinked, and the wire guide could not get through it. The procedure was successfully completed with a bronchoscope, and there were no injuries or additional procedures.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1820334-2018-00875 |
| MDR Report Key | 7374733 |
| Date Received | 2018-03-27 |
| Date of Report | 2018-03-27 |
| Date of Event | 2015-04-21 |
| Date Mfgr Received | 2018-03-23 |
| Device Manufacturer Date | 2015-02-23 |
| Date Added to Maude | 2018-03-27 |
| 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 | MR. LARRY POOL |
| Manufacturer Street | 750 DANIELS WAY |
| Manufacturer City | BLOOMINGTON IN 47404 |
| Manufacturer Country | US |
| Manufacturer Postal | 47404 |
| Manufacturer Phone | 8128294891 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | MELKER EMERGENCY CUFFED CRICOTHYROTOMY CATHETER SET |
| Generic Name | BWC NEEDLE, EMERGENCY AIRWAY |
| Product Code | BWC |
| Date Received | 2018-03-27 |
| Model Number | G29432 |
| Catalog Number | C-TCCSB-500 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COOK INC |
| Manufacturer Address | 750 DANIELS WAY BLOOMINGTON IN 47404 US 47404 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-03-27 |