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

MAUDE Adverse Event Report: MDT POWERED SURGICAL SOLUTIONS MOTOR LEGEND EHS REFURB; DRILLS, BURRS, TREPHINES & ACCESSORIES (COMPOU

  • 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
 

MDT POWERED SURGICAL SOLUTIONS MOTOR LEGEND EHS REFURB; DRILLS, BURRS, TREPHINES & ACCESSORIES (COMPOU Back to Search Results
Model Number EM100-A
Device Problem Overheating of Device (1437)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 12/08/2022
Event Type  malfunction  
Event Description
Repair request initiated for device with the report of overheating. no patient impact was reported.Repair request escalated to a product event due to reason for return.On follow-up it was reported that there was no patient involvement.
 
Manufacturer Narrative
Report confirmed.The device was tested and the temperature was measured to be 146°f.The likely cause of failure could not be determined.It was also noted collet laser markings faded, drive dog pin is broken and the drive dog is worn.Medtronic is submitting this report to comply with fda reporting regulations under 21 cfr parts 4 and 803.This report is based upon information obtained by medtronic, which the company may not have been able to fully investigate or verify prior to the date the report was required by the fda.Medtronic has made reasonable efforts to obtain more complete information and has provided as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.In particular, this report does not constitute an admission by anyone that the product described in this report has any ¿defects¿ or has ¿malfunctioned¿.These words are included in the fda 3500a form and are fixed items for selection created by the fda to categorize the type of event solely for the purpose of regulatory reporting.Medtronic objects to the use of these words and others like them because of the lack of definition and the connotations implied by these terms.This statement should be included with any information or report disclosed to the public under the freedom of information act.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
MOTOR LEGEND EHS REFURB
Type of Device
DRILLS, BURRS, TREPHINES & ACCESSORIES (COMPOU
Manufacturer (Section D)
MDT POWERED SURGICAL SOLUTIONS
4620 north beach street
fort worth TX 76137
Manufacturer (Section G)
MDT POWERED SURGICAL SOLUTIONS
4620 north beach street
fort worth TX 76137
Manufacturer Contact
glen belmer
7000 central avenue ne
ft. worth, TX 76137-3291
6122713209
MDR Report Key16370397
MDR Text Key309495358
Report Number1625507-2023-00040
Device Sequence Number1
Product Code HBF
UDI-Device Identifier00763000096632
UDI-Public00763000096632
Combination Product (y/n)N
Reporter Country CodeNL
PMA/PMN Number
K012456
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign,Health Professional,Company Representative
Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date 02/14/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model NumberEM100-A
Device Catalogue NumberEM100-A
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer12/21/2022
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received 01/17/2023
Initial Date FDA Received02/14/2023
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured09/06/2019
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
-
-