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 2020-01-27 for I/A HANDPIECE TIP 8065750263 manufactured by Alcon Research, Llc - Alcon Precision Device.
[181648225]
This report originally filed as 1644019-2019-00208. The manufacturer internal reference number is: (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[181648226]
A physician reported that a small fragment was detected in a patient's iris at the slit lamp review the day after a cataract procedure.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2523835-2020-00019 |
MDR Report Key | 9632818 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-01-27 |
Date of Report | 2020-01-27 |
Date of Event | 2019-12-02 |
Date Mfgr Received | 2019-12-19 |
Device Manufacturer Date | 2019-04-24 |
Date Added to Maude | 2020-01-27 |
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. JASON MICHAELIDES |
Manufacturer Street | 6201 SOUTH FREEWAY MAIL STOP AB2-6 |
Manufacturer City | FORT WORTH TX 76134 |
Manufacturer Country | US |
Manufacturer Postal | 76134 |
Manufacturer Phone | 8175686438 |
Manufacturer G1 | ALCON RESEARCH, LLC - ALCON PRECISION DEVICE |
Manufacturer Street | 714 COLUMBIA AVENUE |
Manufacturer City | SINKING SPRING PA 19608 |
Manufacturer Country | US |
Manufacturer Postal Code | 19608 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | I/A HANDPIECE TIP |
Generic Name | CATHETER, IRRIGATION |
Product Code | GBX |
Date Received | 2020-01-27 |
Model Number | NA |
Catalog Number | 8065750263 |
Lot Number | 293451M |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ALCON RESEARCH, LLC - ALCON PRECISION DEVICE |
Manufacturer Address | 714 COLUMBIA AVENUE SINKING SPRING PA 19608 US 19608 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-27 |