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

MAUDE Adverse Event Report: SIRONA DENTAL SYSTEMS GMBH MIDWEST E PLUS 1:5 HIGH SPEED CONTRA ANGLE ATTACHMENT; HANDPIECE, AIR-POWERED, DENTAL

  • 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
 

SIRONA DENTAL SYSTEMS GMBH MIDWEST E PLUS 1:5 HIGH SPEED CONTRA ANGLE ATTACHMENT; HANDPIECE, AIR-POWERED, DENTAL Back to Search Results
Catalog Number 875205
Device Problem Overheating of Device (1437)
Patient Problems Burn(s) (1757); No Clinical Signs, Symptoms or Conditions (4582)
Event Type  malfunction  
Event Description
This report summarizes 21 malfunction events where a midwest e plus 1:5 high speed contra angle attachment handpiece overheated.20 events resulted in no injury.1 event resulted in the patient being slightly burned with no intervention.
 
Manufacturer Narrative
Additional serial numbers included in this report: (b)(6).20 of 21 devices were returned for evaluation.We are awaiting the return of 1 device.Evaluation of one device found it to be within specification.Evaluation of 1 device found to have incompatiable component and the turbine needed to be replaced.The device was repaired and returned to the customer.Evaluation of three devices found excessive wear due to a lack of proper maintenance.The devices did not heat up during evaluation.The devices were repaired and returned to the customer.Evaluation of three devices found excessive wear due to a lack of proper maintenance and lubrication.The devices did not heat up during evaluation.The devices were repaired and returned to the customer.Evaluation of two devices found excessive wear due to a lack of proper maintenance and lubrication.A friction problem was identified from pressure on the cap.The devices did not heat up during evaluation.The devices were repaired and returned to the customer.Evaluation of one device found excessive wear due to a lack of proper maintenance and lubrication.The device had debris build-up.A friction problem was identified from pressure on the cap.The device did not heat up during evaluation.The device was repaired and returned to the customer.Evaluation of three devices found excessive wear due to a lack of proper maintenance.A friction problem was identified from pressure on the cap.The devices did not heat up during evaluation.The devices were repaired and returned to the customer.Evaluation of one device found excessive wear due to a lack of proper maintenance.A friction problem was identified from pressure on the cap.This device had a deformation issue (dent).The device did not heat up during evaluation.The device was repaired and returned to the customer.Evaluation of four devices found excessive wear due to a lack of proper maintenance.The devices had debris build-up.The devices did not heat up during evaluation.The devices were repaired and returned to the customer.Evaluation of one device found excessive wear due to a lack of proper maintenance.The devices had debris build-up.A friction problem was identified from pressure on the cap.This device had a deformation issue (dent).The device did not heat up during evaluation.The device was repaired and returned to the customer.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
MIDWEST E PLUS 1:5 HIGH SPEED CONTRA ANGLE ATTACHMENT
Type of Device
HANDPIECE, AIR-POWERED, DENTAL
Manufacturer (Section D)
SIRONA DENTAL SYSTEMS GMBH
fabrikstrasse 31
bensheim, hessen D-646 25
GM  D-64625
Manufacturer (Section G)
SIRONA DENTAL SYSTEMS GMBH
fabrikstrasse 31
bensheim, hessen D-646 25
GM   D-64625
Manufacturer Contact
hannah seevaratnam
221 w. philadelphia st.
york, PA 17401
7178494593
MDR Report Key18556636
MDR Text Key333403827
Report Number9614977-2023-00049
Device Sequence Number1
Product Code EFB
UDI-Device IdentifierE2768752050
UDI-PublicE2768752050
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K972436
Number of Events Reported21
Summary Report (Y/N)Y
Report Source Manufacturer
Reporter Occupation Other
Type of Report Initial
Report Date 01/16/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received01/22/2024
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Catalogue Number875205
Patient Sequence Number1
-
-