MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-15 for SPYGLASS DS M00546650 manufactured by Boston Scientific Corporation.
[175095498]
The spyglass ds digital controller and cable cleaning instructions state to use 15-70% isopropyl alcohol in a purified water solution. The autolith touch states to clean the cable using a moistened cloth. Manufacturer's cleaning instructions are not appropriate for this piece of hospital equipment.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9590843 |
MDR Report Key | 9590843 |
Date Received | 2020-01-15 |
Date of Report | 2019-11-18 |
Date of Event | 2019-11-15 |
Report Date | 2019-11-18 |
Date Reported to FDA | 2019-11-18 |
Date Reported to Mfgr | 2020-01-15 |
Date Added to Maude | 2020-01-15 |
Event Key | 0 |
Report Source Code | User Facility report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 0 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | RISK MANAGER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SPYGLASS DS |
Generic Name | LED LIGHT SOURCE |
Product Code | NTN |
Date Received | 2020-01-15 |
Model Number | M00546650 |
Device Availability | * |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BOSTON SCIENTIFIC CORPORATION |
Manufacturer Address | 300 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 US 01752 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-15 |