BASIC VENTURI PHACO PACK DP4305E

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2005-11-03 for BASIC VENTURI PHACO PACK DP4305E manufactured by Bausch & Lomb, Inc..

Event Text Entries

[405735] Aspiration problems during the procedure resulted in the need to perform an extracapsular procedure. A stitch was required to close the wound. There was no additional pt injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1920664-2005-00113
MDR Report Key644306
Report Source05,07
Date Received2005-11-03
Date of Report2005-10-03
Date of Event2005-09-28
Date Mfgr Received2005-10-03
Device Manufacturer Date2005-06-01
Date Added to Maude2005-11-04
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 Location0
Manufacturer ContactJACKIE FLACH
Manufacturer Street3365 TREE COURT IND. BLVD.
Manufacturer CityST. LOUIS MO 63122
Manufacturer CountryUS
Manufacturer Postal63122
Manufacturer Phone6362263255
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBASIC VENTURI PHACO PACK
Generic NameOPTHTHALMIC MICROSURGICAL ACCESSORY PACK
Product CodeMSR
Date Received2005-11-03
Model NumberNA
Catalog NumberDP4305E
Lot NumberT5662
ID NumberNA
Device Expiration Date2007-05-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key633794
ManufacturerBAUSCH & LOMB, INC.
Manufacturer Address* ROCHESTER NY 14609 US
Baseline Brand NameBASIC VENTURI PHACO PACK
Baseline Generic NameOPHTHALMIC MICROSURGICAL ACCESSORY PACK
Baseline Model NoNA
Baseline Catalog NoDP4305E
Baseline IDNA
Baseline Device FamilyNA
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK980100
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2005-11-03

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