SYMMETRY SHARP KERRISON TIP 53-1661

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-22 for SYMMETRY SHARP KERRISON TIP 53-1661 manufactured by Symmetry Surgical Inc..

Event Text Entries

[118115775] During the acdf (anterior cervical discectomy and fusion), the symmetry sharp kerrison tip broke off. The surgeon ordered an x-ray. The symmetry sharp kerrison tip could not be identified in the x-ray. The symmetry sharp kerrison tip could not be found in the surgical field. The patient was sent to recovery in stable condition. No untoward effects.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3007208013-2018-00015
MDR Report Key7807021
Date Received2018-08-22
Date of Report2018-08-22
Date of Event2018-06-01
Date Mfgr Received2018-08-02
Date Added to Maude2018-08-22
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. VICTORIA ROGERS
Manufacturer Street3034 OWEN DRIVE
Manufacturer CityANTIOCH TN 37013
Manufacturer CountryUS
Manufacturer Postal37013
Manufacturer Phone8002513000
Manufacturer G1SYMMETRY SURGICAL INC.
Manufacturer Street3034 OWEN DRIVE
Manufacturer CityANTIOCH TN 37013
Manufacturer CountryUS
Manufacturer Postal Code37013
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSYMMETRY SHARP KERRISON TIP
Generic NameRONGEUR TIP
Product CodeHAE
Date Received2018-08-22
Model Number53-1661
Catalog Number53-1661
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSYMMETRY SURGICAL INC.
Manufacturer Address3034 OWEN DRIVE ANTIOCH TN 37013 US 37013


Patients

Patient NumberTreatmentOutcomeDate
10 2018-08-22

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