MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-02-19 for FIBER OPTIC ILLUMINATOR 8065751577 manufactured by Alcon Research, Llc - Houston.
[183727291]
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. The manufacturer internal reference number is: (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[183727292]
A customer reported that the green ring of the trocar cannula came off the shaft during a procedure. The product was replaced and the procedure was completed. There was no patient harm.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1644019-2020-00097 |
MDR Report Key | 9730983 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-02-19 |
Date of Report | 2020-02-19 |
Date of Event | 2020-01-29 |
Date Mfgr Received | 2020-01-30 |
Device Manufacturer Date | 2019-09-11 |
Date Added to Maude | 2020-02-19 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 0 |
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 | FIBER OPTIC ILLUMINATOR |
Generic Name | LIGHT, SURGICAL, FIBEROPTIC |
Product Code | FST |
Date Received | 2020-02-19 |
Model Number | NA |
Catalog Number | 8065751577 |
Lot Number | 2318836H |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
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 | 2020-02-19 |