PUREPOINT LASER 8065751481

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-05-29 for PUREPOINT LASER 8065751481 manufactured by Alcon Research, Llc - Irvine Technology Center.

Event Text Entries

[146665950] 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


[146665951] A customer reported that during a procedure, laser beaming was interrupted frequently. The system could be restarted and the procedure could begin again. There were no error messages displayed. The customer suspects a problem with the footswitch. Additional information is not expected.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2028159-2019-00957
MDR Report Key8650156
Date Received2019-05-29
Date of Report2019-07-31
Date of Event2019-04-04
Date Mfgr Received2019-07-09
Device Manufacturer Date2018-11-06
Date Added to Maude2019-05-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. CINDY MILAM
Manufacturer Street6201 SOUTH FREEWAY MAIL STOP AB2-6
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal76134
Manufacturer Phone8176152231
Manufacturer G1ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER
Manufacturer Street15800 ALTON PARKWAY
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal Code92618
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report0

Device Details

Brand NamePUREPOINT LASER
Generic NameLASER, OPHTHALMIC
Product CodeHQF
Date Received2019-05-29
Model NumberNA
Catalog Number8065751481
Lot NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER
Manufacturer Address15800 ALTON PARKWAY IRVINE CA 92618 US 92618


Patients

Patient NumberTreatmentOutcomeDate
10 2019-05-29

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