ACCURUS 400 VS 8065740238

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 2012-06-08 for ACCURUS 400 VS 8065740238 manufactured by Alcon - Irvine Technology Center.

Event Text Entries

[2765530] A customer reported that the equipment displayed deficient aspiration and fluid/gas exchange failure during a vitrectomy procedure. After a delay of more than 15 minutes, the case was able to be completed with the same equipment. Add'l info has been requested.
Patient Sequence No: 1, Text Type: D, B5


[9920761] Investigation including root cause analysis, is in progress. A supplemental mdr will be filed as necessary in accordance with 21 cfr 803. 56 when add'l reportable info becomes available. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2028159-2012-00838
MDR Report Key2617337
Report Source01,05
Date Received2012-06-08
Date of Report2012-05-10
Date of Event2012-04-26
Date Mfgr Received2012-05-10
Device Manufacturer Date2008-05-01
Date Added to Maude2012-09-12
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 FDA0
Event Location0
Manufacturer ContactPAUL NITSCHMANN
Manufacturer Street6201 SOUTH FREEWAY, R3-16
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal76134
Manufacturer Phone8176152440
Manufacturer G1ALCON - IRVINE TECHNOLOGY CENTER
Manufacturer Street15800 ALTON PKWY.
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal Code92618
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameACCURUS 400 VS
Generic NamePHACOFRAGMENTATION SYSTEM
Product CodeHLM
Date Received2012-06-08
Model NumberACCURUS
Catalog Number8065740238
Lot NumberNA
ID Number4.54
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALCON - IRVINE TECHNOLOGY CENTER
Manufacturer Address15800 ALTON PKWY. IRVINE CA 92618 US 92618


Patients

Patient NumberTreatmentOutcomeDate
10 2012-06-08

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