MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-10 for GRIESHABER REVOLUTION DSP SCISSORS 706.52 manufactured by Alcon Grieshaber Ag.
[185708885]
No sample has been received by manufacturing for evaluation. 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
[185708886]
A nurse reported that an ophthalmic scissors tip broke off inside of a patient's eye during surgery. No patient impact or harm was reported. Additional information has been requested.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3003398873-2020-00022 |
MDR Report Key | 9811189 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-03-10 |
Date of Report | 2020-03-10 |
Date Mfgr Received | 2020-02-25 |
Device Manufacturer Date | 2019-04-02 |
Date Added to Maude | 2020-03-10 |
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 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 | 3 |
Brand Name | GRIESHABER REVOLUTION DSP SCISSORS |
Generic Name | SCISSORS, OPHTHALMIC |
Product Code | HNF |
Date Received | 2020-03-10 |
Model Number | NA |
Catalog Number | 706.52 |
Lot Number | F176012 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
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 | 2020-03-10 |