IMPLANTABLE COLLAMER LENS (ICL) VTICMO13.2 N/A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,o report with the FDA on 2020-03-23 for IMPLANTABLE COLLAMER LENS (ICL) VTICMO13.2 N/A manufactured by Staar Surgical Company.

Event Text Entries

[188880366] This product is not marketed in the us. (b)(4). No similar complaint type events were reported for units within the same lot. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[188880367] The reporter indicated that a 13. 2mm, vticmo13. 2, -12/+3/108 (sphere/cylinder/axis), implantable collamer lens was implanted into the patients right eye (od) on (b)(6) 2015. Low vault with rotaion was observed. Repositioning of the lens was performed several time but it did not resolve the problem. Lens remains implanted, surgeon plans to exchange lens. If additional information is received a supplemental medwatch report will be submitted.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2023826-2020-00635
MDR Report Key9869647
Report SourceFOREIGN,HEALTH PROFESSIONAL,O
Date Received2020-03-23
Date of Report2020-02-24
Date of Event2020-02-20
Date Mfgr Received2020-02-24
Device Manufacturer Date2014-08-18
Date Added to Maude2020-03-23
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. CYNTHIA THAI
Manufacturer Street1911 WALKER AVENUE
Manufacturer CityMONROVIA, CA
Manufacturer CountryUS
Manufacturer G1STAAR SURGICAL COMPANY
Manufacturer Street1911 WALKER AVENUE
Manufacturer CityMONROVIA, CA
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIMPLANTABLE COLLAMER LENS (ICL)
Generic NamePHAKIC TORIC INTRAOCULAR LENS
Product CodeQCB
Date Received2020-03-23
Model NumberVTICMO13.2
Catalog NumberN/A
Lot NumberN/A
Device Expiration Date2017-07-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTAAR SURGICAL COMPANY
Manufacturer Address1911 WALKER AVENUE MONROVIA, CA US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-23

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