PEERLESS POST 977-1052

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-01-18 for PEERLESS POST 977-1052 manufactured by Sybronendo.

Event Text Entries

[133693437] 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


[133693438] A complainant alleged the post broke and tooth was pulled out. No additional information provided.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2016150-2019-00001
MDR Report Key8263006
Date Received2019-01-18
Date of Report2019-01-18
Date of Event2018-12-03
Date Mfgr Received2019-01-18
Date Added to Maude2019-01-18
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactMR. PAULO CALLE
Manufacturer Street1717 W COLLINS AVENUE
Manufacturer CityORANGE CA 92867
Manufacturer CountryUS
Manufacturer Postal92867
Manufacturer Phone7145167472
Manufacturer G1SYBRONENDO
Manufacturer Street1332 SOUTH LONE HILL AVENUE
Manufacturer CityGLENDORA CA 91740
Manufacturer CountryUS
Manufacturer Postal Code91740
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NamePEERLESS POST
Generic NameROOT CANAL POST
Product CodeELR
Date Received2019-01-18
Catalog Number977-1052
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSYBRONENDO
Manufacturer Address1332 SOUTH LONE HILL AVENUE GLENDORA CA 91740 US 91740


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-01-18

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