MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-12-30 for CONSTELLATION ULTRAVIT PROBE 8065750949 manufactured by Alcon Research, Llc - Houston.
[177935234]
Investigation including root cause analysis is in progress. A supplemental mdr will be filed as necessary in accordance with 21 cfr 803. 56 when additional reportable information becomes available. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[177935235]
A nurse reported the vitrectomy probe was not cutting and the aspiration was working during a vitrectomy procedure. The procedure was completed after the product was replaced with another one. There was no harm to the patient.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1644019-2019-00211 |
MDR Report Key | 9532401 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2019-12-30 |
Date of Report | 2020-03-16 |
Date of Event | 2019-12-09 |
Date Mfgr Received | 2020-03-03 |
Device Manufacturer Date | 2018-03-20 |
Date Added to Maude | 2019-12-30 |
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. JONATHAN SCHLECH |
Manufacturer Street | 6201 SOUTH FREEWAY MAIL STOP AB2-6 |
Manufacturer City | FORT WORTH TX 76134 |
Manufacturer Country | US |
Manufacturer Postal | 76134 |
Manufacturer Phone | 8175514979 |
Manufacturer G1 | ALCON RESEARCH, LLC - HOUSTON |
Manufacturer Street | 9965 BUFFALO SPEEDWAY |
Manufacturer City | HOUSTON TX 77054 |
Manufacturer Country | US |
Manufacturer Postal Code | 77054 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CONSTELLATION ULTRAVIT PROBE |
Generic Name | VITRECTOMY, INSTRUMENT CUTTER |
Product Code | MLZ |
Date Received | 2019-12-30 |
Model Number | NA |
Catalog Number | 8065750949 |
Lot Number | 2126167H |
Device Expiration Date | 2020-01-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ALCON RESEARCH, LLC - HOUSTON |
Manufacturer Address | 9965 BUFFALO SPEEDWAY HOUSTON TX 77054 US 77054 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-12-30 |