GRIESHABER SCISSORS/TIPS, UNSPECIFIED

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-08-23 for GRIESHABER SCISSORS/TIPS, UNSPECIFIED manufactured by Alcon Grieshaber Ag.

Event Text Entries

[53709875] 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. Additional information has been requested. The manufacturer internal reference number is: (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[53709876] A customer reported that five ophthalmic scissors would not move to the closed position during surgery. There was no impact to the patient. Additional information has been requested.
Patient Sequence No: 1, Text Type: D, B5


[53721848] (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3003398873-2016-00012
MDR Report Key5897072
Date Received2016-08-23
Date of Report2016-08-24
Date Mfgr Received2016-08-23
Device Manufacturer Date2015-08-28
Date Added to Maude2016-08-23
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. RITA LOPEZ
Manufacturer Street6201 SOUTH FREEWAY MAIL STOP AB2-6
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal76134
Manufacturer Phone8175514846
Manufacturer G1ALCON GRIESHABER AG
Manufacturer StreetWINKELRIEDSTRASSE 52
Manufacturer CitySCHAFFHAUSEN 8203
Manufacturer CountrySZ
Manufacturer Postal Code8203
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameGRIESHABER SCISSORS/TIPS, UNSPECIFIED
Generic NameSCISSORS, OPHTHALMIC
Product CodeHNF
Date Received2016-08-23
Model NumberNA
Catalog NumberASKU
Lot NumberF126200
Device Expiration Date2018-04-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALCON GRIESHABER AG
Manufacturer AddressWINKELRIEDSTRASSE 52 SCHAFFHAUSEN 8203 SZ 8203


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2016-08-23

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