MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-09-28 for UROPASS AS 12/14FR X 38 CM 5/BX 61238BX manufactured by Teleflex Medical Oem.
[122197119]
The device was not returned to olympus for evaluation. The cause of the reported event could not be confirmed at this time. In addition, there is insufficient information regarding the reported device, patient and procedure. Multiple follow ups were made to the user facility, however, no additional information was obtained. Olympus will continue to investigate this complaint to obtain more detailed information regarding the reported event. If additional information becomes available, this report will be updated and supplemented accordingly.
Patient Sequence No: 1, Text Type: N, H10
[122197120]
Olympus was informed that during a therapeutic procedure, the device broke off and became stuck inside the patient. The user facility also reported it was the second time the reported event has occurred, the last time was about three weeks ago. Two of 2 reports
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2951238-2018-00586 |
| MDR Report Key | 7920908 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2018-09-28 |
| Date of Report | 2018-10-26 |
| Date Mfgr Received | 2018-10-05 |
| Date Added to Maude | 2018-09-28 |
| 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 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MS. CONNIE TUBERA |
| Manufacturer Street | 2400 RINGWOOD AVENUE |
| Manufacturer City | SAN JOSE CA 95131 |
| Manufacturer Country | US |
| Manufacturer Postal | 95131 |
| Manufacturer Phone | 4089355124 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | UROPASS AS 12/14FR X 38 CM 5/BX |
| Generic Name | UROPASS ACCESS SHEATH |
| Product Code | KNY |
| Date Received | 2018-09-28 |
| Model Number | 61238BX |
| Catalog Number | 61238BX |
| Lot Number | 09G1400007 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | TELEFLEX MEDICAL OEM |
| Manufacturer Address | 3750 ANNAPOLIS LANE NORTH, SUITE 160 PLYMOUTH MN 55447 US 55447 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-09-28 |