• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NAKANISHI INC. NSK; HANDPIECE, ROTARY BONE CUTTING

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

NAKANISHI INC. NSK; HANDPIECE, ROTARY BONE CUTTING Back to Search Results
Model Number SGS-E2S
Device Problem Overheating of Device (1437)
Patient Problems Burn(s) (1757); Partial thickness (Second Degree) Burn (2694)
Event Date 03/11/2022
Event Type  Injury  
Manufacturer Narrative
The same adverse event in this report has been reported to the fda separately by the distributor, (b)(4), under report number (b)(4).The dentist refused to provide the patient's ethnicity and race.
 
Event Description
On march 17, 2022, nakanishi became aware of a handpiece overheating through a complaint input into the complaint database by a distributor ((b)(4)).Details are as follows: the event occurred on (b)(6) 2022.The dentist was performing a 3rd molar extraction on a patient using the sgs-e2s handpiece (serial no.(b)(4)).During the procedure, the handpiece overheated and the patient received a minor burn injury.It was reported that the patient has had a follow up visit and no additional medical treatment was required for the injury.
 
Manufacturer Narrative
Upon receiving the device involved in the mdr event from the distributor, nakanishi conducted a failure analysis of the returned device, which included measuring the operating temperature of the device [report no.(b)(4)].These activities are described in more detail below.Methodology used: a) nakanishi examined the device history record and the repair history for the subject sgs-e2s device [serial no.(b)(6)].There were no problems observed during manufacturing or testing noted in the dhr.There were also no repair history records since the device was shipped.B) nakanishi conducted temperature testing of the returned device in the following manner: b.1) temperature sensors were attached to the exterior of the device at various test points.This included the point most proximal to the patient (testing point (1) and points further toward the distal end of the device (testing points (2) through (4).The test setup was prepared to take temperature measurements at all points simultaneously, including a reference measurement at ambient room temperature.B.2) nakanishi attached a thermocouple (sensor to measure temperature) to each of the testing points.Nakanishi rotated the device's motor at 40,000 min-1, which is the maximum rpm for the motor that drives the handpiece (80,000 min-1 for the handpiece), with no water spray, and measured the exothermic response.B.3) nakanishi measured the temperature rise of the returned handpiece set at 80,000 min-1 (motor revolution 40,000 min-1).Nakanishi observed an abnormal temperature rise at test points (1) and (2) a few seconds into the test.Temperature measurements about 50 seconds after the start of the test were as follows: test point (1): 102.4 degrees c, test point (2): 52.3 degrees c, test point (3): 35.3 degrees c, test point (4): 45.9 degrees c.The increase in temperature was so sudden that the test was concluded about 50 seconds into the planned 5-minute evaluation period.Identification of the specific failure mode(s) and/or mechanism(s) of the associated device components was conducted as follows: a) nakanishi disassembled the handpiece and performed a visual inspection of the internal parts.Nakanishi observed that the bearing was broken, discolored, and soiled.B) nakanishi took photographs of all the disassembled parts and kept them in investigation report no.(b)(4).Conclusions reached based on the investigation and analysis results: a) nakanishi determined that the cause of the overheating of the returned device was abnormal resistance during rotation due to the broken bearing.Nakanishi considers the possibility from many years of experience that the cause of the broken bearing was the ingress of undesirable materials into the bearing, leading to abrasion.B) a lack of maintenance caused the accumulation of debris on the internal parts, which caused debris ingress into the bearing during rotation.This contributed to the handpiece overheating.C) in order to prevent a recurrence of the handpiece overheating, nakanishi took the following actions: c.1) nakanishi reviewed the operation manual and reconfirmed the clarity and understandability of the instructions.C.2) nakanishi reported the above evaluation results to nsk america and directed nsk america to remind the user of the importance of maintenance, as instructed in the operation manual.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
NSK
Type of Device
HANDPIECE, ROTARY BONE CUTTING
Manufacturer (Section D)
NAKANISHI INC.
700 shimohinata
kanuma-shi, tochigi-ken 322-8 666
JA  322-8666
Manufacturer (Section G)
NAKANISHI INC.
700 shimohinata
kanuma-shi, tochigi-ken 322-8 666
JA   322-8666
Manufacturer Contact
sean kaufman
1800 global parkway
hoffman estates, IL 60192
2245128921
MDR Report Key14100479
MDR Text Key289199643
Report Number9611253-2022-00020
Device Sequence Number1
Product Code KMW
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K171155
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Company Representative,Distributor
Reporter Occupation Physician Assistant
Remedial Action Recall
Type of Report Initial,Followup
Report Date 05/19/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received04/13/2022
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model NumberSGS-E2S
Device Catalogue NumberH266
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer04/07/2022
Is the Reporter a Health Professional? Yes
Date Manufacturer Received04/25/2022
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured08/28/2017
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Removal/Correction Number9611253-060818-001-R
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age16 YR
Patient SexFemale
Patient Weight61 KG
-
-