Streamline Surgical System
Received Jul 27, 2026
Report 1000125279-2026-00031 · MDR key 50010864
Device
Generic name
Infusion Pump
Manufacturer
New World Medical, Inc.Model number
StreamlineCatalog number
Streamline
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
Not reported
- Hemorrhage/Blood Loss/Bleeding
Narrative
Description of Event or Problem
Dr. (b)(6) had a good first procedure. There was some excess blood, likely from slightly too much pressure. He is looking forward to the second case in two weeks and wants to make a more permanent switch away from iStent.
Additional Manufacturer Narrative
The IFU for the reported product model was reviewed and confirmed to include that blood reflux into the anterior chamber may be expected during use of the device.The Device History Record (DHR) could not be reviewed, as no specific serial or lot information was available. The product was manufactured, tested, and released in accordance with validated procedures.As the device is not available for return, no device malfunction could be confirmed.