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

MAUDE Adverse Event Report: STRYKER GMBH SCREWDRIVER BIT AXSOS T15, AO FITTING 4.0MM LOCKING SET; ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

  • 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
 

STRYKER GMBH SCREWDRIVER BIT AXSOS T15, AO FITTING 4.0MM LOCKING SET; ORTHOPEDIC MANUAL SURGICAL INSTRUMENT Back to Search Results
Model Number 702753
Medical Device Problem Codes Break (1069); Material Deformation (2976)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 03/11/2021
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
Upon completion of investigation, additional information will be provided in a supplemental report.
 
Event or Problem Description
As reported: "the tips of 2 screwdrivers were damaged when the proximal plate of the axos tibia was pulled out.The screw was able to removed with a driver of the same standard of other company in the deformation of the screw could not be confirmed in the photo before removal.It was confirmed no residual remained inside the body.The catalog no.Of screw is unknown.".
 
Event or Problem Description
As reported: "the tips of 2 screwdrivers were damaged when the proximal plate of the axos tibia was pulled out.The screw was able to removed with a driver of the same standard of other company in the deformation of the screw could not be confirmed in the photo before removal.It was confirmed no residual remained inside the body.The catalog no.Of screw is unknown.".
 
Additional Manufacturer Narrative
The reported event could be confirmed, since the device was returned for evaluation and matches the reported failure mode.Device inspection revealed the following: the received screwdriver bit shows signs of normal and prolonged usage however its tip is found to be broken.The breakage surface shows signs of slight rotational deformation/waves.Absence of plastic deformation and presence of an uneven breakage indicates that the breakage was instantaneous due to high torsional and bending overload.However, it cannot be excluded that residual stress from previous usage may have also contributed in the breakage.The average hardness of the drill was observed to be 61.8 hrc as required against a range of 58.0 hrc ¿ 62.0 hrc.The returned screwdriver bit was found to be within specifications.A review of the device history for the reported lot did not indicate any abnormalities.No corrective actions are required at this time.No indications of manufacturing or design related problems were found during the investigation.A review of the labeling did not indicate any abnormalities.If any further information is provided, the complaint report will be updated.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
SCREWDRIVER BIT AXSOS T15, AO FITTING 4.0MM LOCKING SET
Common Device Name
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
Manufacturer (Section D)
STRYKER GMBH
bohnackerweg 1
postfach
selzach 2545
SZ  2545
MDR Report Key11602880
Report Number0008031020-2021-00118
Device Sequence Number11875912
Product Code LXH
UDI-Device Identifier07613327005028
UDI-Public07613327005028
Combination Product (Y/N)N
Initial Reporter CountryJA
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source health professional
Initial Reporter Occupation Physician
Type of Report Initial,Followup
Report Date (Section B) 06/25/2021
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
Operator of Device Health Professional
Device Model Number702753
Device Catalogue Number702753
Device Lot NumberJ03885
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer04/13/2021
Initial Date Received by Manufacturer 03/11/2021
Supplement Date Received by Manufacturer06/04/2021
Initial Report FDA Received Date04/01/2021
Supplement Report FDA Received Date06/25/2021
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
-
-