MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2018-04-27 for FLEXOR PARALLEL URETERAL ACCESS SHEATH AND DILATORS FUS-107045-P manufactured by Cook Inc.
[106974110]
(b)(4). This report includes information known at this time.? A follow-up report will be submitted should additional relevant information become available.
Patient Sequence No: 1, Text Type: N, H10
[106974111]
It was reported that the user used the parallel option of the flexor parallel ureteral access sheath and dilators. While using a non cook coloplast wire, the wire changed its form and separated due to the sharp hole for the parallel function of the flexor. The physician retrieved the three sections of wire from the patient. The patient was not hurt. A section of the device did not remain inside the patient? S body. The patient did not require any additional procedures due to this occurrence.? According to the initial reporter, the patient did not experience any adverse effects due to this occurrence.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1820334-2018-01192 |
| MDR Report Key | 7468545 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2018-04-27 |
| Date of Report | 2018-07-20 |
| Date of Event | 2018-03-29 |
| Date Mfgr Received | 2018-07-19 |
| Device Manufacturer Date | 2018-01-17 |
| Date Added to Maude | 2018-04-27 |
| 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 | 8123392235 |
| 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 | 3 |
| Brand Name | FLEXOR PARALLEL URETERAL ACCESS SHEATH AND DILATORS |
| Generic Name | KOE DILATOR, URETHRAL |
| Product Code | KOE |
| Date Received | 2018-04-27 |
| Returned To Mfg | 2018-05-09 |
| Catalog Number | FUS-107045-P |
| Lot Number | 8516256 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| 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 | 1. Required No Informationntervention | 2018-04-27 |