MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-04-24 for GRIESHABER REVOLUTION DSP SCISSORS 705.52P manufactured by Alcon Grieshaber Ag.
[143225078]
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
[143225079]
A customer report that the scissors made a "click" sound and they did not close all the way before a vitrectomy procedure. There was no patient involvement.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3003398873-2019-00028 |
MDR Report Key | 8547374 |
Date Received | 2019-04-24 |
Date of Report | 2019-05-29 |
Date of Event | 2019-02-19 |
Date Mfgr Received | 2019-04-30 |
Device Manufacturer Date | 2016-08-17 |
Date Added to Maude | 2019-04-24 |
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 | MS. CINDY MILAM |
Manufacturer Street | 6201 SOUTH FREEWAY MAIL STOP AB2-6 |
Manufacturer City | FORT WORTH TX 76134 |
Manufacturer Country | US |
Manufacturer Postal | 76134 |
Manufacturer Phone | 8176152231 |
Manufacturer G1 | ALCON GRIESHABER AG |
Manufacturer Street | WINKELRIEDSTRASSE 52 |
Manufacturer City | SCHAFFHAUSEN 8203 |
Manufacturer Country | SZ |
Manufacturer Postal Code | 8203 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 0 |
Brand Name | GRIESHABER REVOLUTION DSP SCISSORS |
Generic Name | SCISSORS, OPHTHALMIC |
Product Code | HNF |
Date Received | 2019-04-24 |
Returned To Mfg | 2019-04-25 |
Model Number | NA |
Catalog Number | 705.52P |
Lot Number | F140797 |
Device Expiration Date | 2019-07-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ALCON GRIESHABER AG |
Manufacturer Address | WINKELRIEDSTRASSE 52 SCHAFFHAUSEN 8203 SZ 8203 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-04-24 |