MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2016-02-27 for MERGE EYE STATION 10.6.61 manufactured by Merge Healthcare.
[39204186]
Based upon the available information, the cause for the reported event was likely due to a human factors issue. There is no indication that the reported event was related to product malfunction or defect.
Patient Sequence No: 1, Text Type: N, H10
[39204187]
Merge eye station is intended to be used in conjunction with existing ophthalmic fundus cameras to take images of the eye, perform fluorescein angiography, red free, color and icg still-image photography as well as video imaging. Merge healthcare was notified that images were accidentally deleted by a customer while trying to edit a patient's information in the database. The accidental deletion of images could potentially lead to a delay in diagnosis or treatment. The customer also indicated that the accidentally deleted images were for a patient with a retinal tear. The patient received the necessary treatment for the retinal tear and the procedure was completed successfully.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2183926-2016-00452 |
| MDR Report Key | 5465392 |
| Report Source | USER FACILITY |
| Date Received | 2016-02-27 |
| Date of Report | 2016-02-27 |
| Date of Event | 2016-01-29 |
| Date Mfgr Received | 2016-01-29 |
| Date Added to Maude | 2016-02-27 |
| 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 |
| Reporter Occupation | PHYSICIAN ASSISTANT |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR. MICHAEL DIEDRICK |
| Manufacturer Street | 900 WALNUT RIDGE DR. |
| Manufacturer City | HARTLAND WI 53029 |
| Manufacturer Country | US |
| Manufacturer Postal | 53029 |
| Manufacturer Phone | 2629123570 |
| Manufacturer G1 | MERGE HEALTHCARE |
| Manufacturer Street | 900 WALNUT RIDGE DRIVE |
| Manufacturer City | HARTLAND, WI 53029 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 53029 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | MERGE EYE STATION |
| Generic Name | CAMERA, OPHTHALMIC, AC-POWERED |
| Product Code | NFJ |
| Date Received | 2016-02-27 |
| Model Number | MERGE EYE STATION |
| Catalog Number | 10.6.61 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MERGE HEALTHCARE |
| Manufacturer Address | 900 WALNUT RIDGE DRIVE HARTLAND, WI 53029 US 53029 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2016-02-27 |