MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-09 for WM-NP2 WORKSTATION SET 3 (ROW) K10020681 manufactured by Keymed (medical And Industrial Equipment) Ltd..
[117013388]
Broken castor was discovered when the workstation was returned to olympus (b)(4). There has been no report of injury to patient or user. Olympus keymed have requested the workstation and castor is returned for further investigation. Follow up report will be submitted once the keymed investigation has been completed.
Patient Sequence No: 1, Text Type: N, H10
[117013389]
The left castor has broken off from the workstation. The workstation was lent to the customer, when the customer returned it the malfunction was found during "receipt inspection" at olympus.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9611174-2018-00013 |
| MDR Report Key | 7766620 |
| Date Received | 2018-08-09 |
| Date of Report | 2018-10-17 |
| Date of Event | 2018-07-23 |
| Date Mfgr Received | 2018-10-16 |
| Device Manufacturer Date | 2014-10-07 |
| Date Added to Maude | 2018-08-09 |
| 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 PETER MORCOS |
| Manufacturer Street | KEYMED HOUSE, STOCK ROAD |
| Manufacturer City | SOUTHEND ON SEA, ESSEX SS25QH |
| Manufacturer Country | UK |
| Manufacturer Postal | SS25QH |
| Manufacturer Phone | 0441702616 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | WM-NP2 WORKSTATION SET 3 (ROW) |
| Generic Name | WM-*P2 SERIES OF ENDOSCOPY WORKSTATIONS |
| Product Code | FEM |
| Date Received | 2018-08-09 |
| Returned To Mfg | 2018-08-06 |
| Model Number | K10020681 |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | KEYMED (MEDICAL AND INDUSTRIAL EQUIPMENT) LTD. |
| Manufacturer Address | KEYMED HOUSE, STOCK ROAD SOUTHEND-ON-SEA, ESSEX US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-08-09 |