MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-04-11 for DESILETS-HOFFMAN INTRODUCER SET G18089 DHIS-080030-RB-DIL88 manufactured by Cook Inc.
[105519554]
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
[105519555]
It was reported that during a demonstration of the desilets-hoffman introducer set, fine strands of an unknown material began protruding from the van-andel end of the 8fr dilator. There was no patient involvement, so there were no injuries or additional procedures reported.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1820334-2018-01119 |
| MDR Report Key | 7422352 |
| Date Received | 2018-04-11 |
| Date of Report | 2018-04-11 |
| Date of Event | 2016-07-12 |
| Date Mfgr Received | 2018-04-09 |
| Device Manufacturer Date | 2016-05-02 |
| Date Added to Maude | 2018-04-11 |
| 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 | 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 | DESILETS-HOFFMAN INTRODUCER SET |
| Generic Name | KOE DILATOR, URETHRAL |
| Product Code | KOE |
| Date Received | 2018-04-11 |
| Model Number | G18089 |
| Catalog Number | DHIS-080030-RB-DIL88 |
| 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 | 2018-04-11 |