MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-12-18 for WAYNE PNEUMOTHORAX TRAY C-UTPTY-1400-WAYNE-112497 manufactured by Cook Inc.
[131143747]
This mdr is being filed after the associated complaint was reviewed under remediation protocol (b)(4), 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
[131143748]
The complainant reported that a patient in the ed (emergency department) needed a chest tube for a pneumothorax, and there was substantial difficulty with the wayne pneumothorax tray. The kits (two lot numbers: this mfr# and related mfr# 1820334-2018-03816) had kinks and frays in the guide wire that made it impossible to thread the chest tube into the chest cavity for pneumothorax drainage. It took 6 attempts to insert a chest tube into the patient, and the patient was awaiting ir for placement of a small chest tube. The physicians all attempted various ways/ workarounds with the only success being placing a pediatric tube for temporary inflation of the patient's lung. After xr (x-ray) confirmation, it was determined that a larger chest tube was necessary. Hence a subsequent attempt and failure. These product problem did not result in any reported serious injuries to the patient.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1820334-2018-03815 |
| MDR Report Key | 8176830 |
| Date Received | 2018-12-18 |
| Date of Report | 2018-12-18 |
| Date of Event | 2015-08-15 |
| Date Mfgr Received | 2018-12-14 |
| Device Manufacturer Date | 2015-04-13 |
| Date Added to Maude | 2018-12-18 |
| 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 | 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 |
| Manufacturer G1 | COOK INC |
| Manufacturer Street | 750 DANIELS WAY |
| Manufacturer City | BLOOMINGTON IN 47404 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 47404 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | WAYNE PNEUMOTHORAX TRAY |
| Generic Name | DQR CANNULA, CATHETER |
| Product Code | DQR |
| Date Received | 2018-12-18 |
| Returned To Mfg | 2015-10-01 |
| Model Number | NA |
| Catalog Number | C-UTPTY-1400-WAYNE-112497 |
| Lot Number | 5747374 |
| Device Expiration Date | 2017-03-30 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| 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 | 2018-12-18 |