OPTIVIEW 716-0050

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-10-18 for OPTIVIEW 716-0050 manufactured by Kerr Hawe S.a.

Event Text Entries

[163007298] Patient went to the emergency room where patient received intramuscular injection of steroid. Additionally, patient received oral steroid encorton, solcoseryl for lubrication and the rinse eludril. Currently patient is doing well and has no complaints. Specific patient information with regards to ethnicity, race and weight was not provided. No lot number was provided therefore manufacture date cannot be determined. The product was not returned and no lot number or part number was provided; therefore, no evaluation can be conducted.
Patient Sequence No: 1, Text Type: N, H10


[163007299] A complainant alleged that two (2) patients experienced an allergic reaction resulting in swellings, burning and pain in lips. This is the first of two reports.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8031023-2019-00001
MDR Report Key9206080
Report SourceHEALTH PROFESSIONAL
Date Received2019-10-18
Date of Report2019-10-17
Date Mfgr Received2019-09-19
Date Added to Maude2019-10-18
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. PAULO CALLE
Manufacturer Street1717 W COLLINS AVE
Manufacturer CityORANGE CA 92867
Manufacturer CountryUS
Manufacturer Postal92867
Manufacturer Phone7145167752
Manufacturer G1KERR HAWE S.A
Manufacturer StreetVIA STRECCE 4
Manufacturer CityBIOGGIO, 6934
Manufacturer CountrySZ
Manufacturer Postal Code6934
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOPTIVIEW
Generic NameLIP AND CHEEK RETRACTOR
Product CodeEIG
Date Received2019-10-18
Catalog Number716-0050
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerKERR HAWE S.A
Manufacturer AddressVIA STRECCE 4 BIOGGIO, 6934 SZ 6934


Patients

Patient NumberTreatmentOutcomeDate
101. Other; 2. Required No Informationntervention 2019-10-18

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