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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STRYKER GMBH STANDARD BARREL HIP PLATE, KEYED OMEGA 3 135°, 4 HOLES; APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

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STRYKER GMBH STANDARD BARREL HIP PLATE, KEYED OMEGA 3 135°, 4 HOLES; APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT Back to Search Results
Model Number 597024S
Device Problem Device Contaminated During Manufacture or Shipping (2969)
Patient Problem Insufficient Information (4580)
Event Date 01/15/2022
Event Type  malfunction  
Event Description
The customer reported a foreign body in an omega implant box.
 
Manufacturer Narrative
Upon completion of investigation, additional information will be provided in a supplemental report.
 
Event Description
The customer reported a foreign body in an omega implant box.
 
Manufacturer Narrative
The reported event could not be confirmed since the original packaging was not returned and since the complete packaging is not visible on the received pictures.The device inspection revealed the following: a steel ball with a diameter of 1.98mm was returned for evaluation.The ball has no markings or any other identifying features on it.The original package and the implant were not returned for evaluation.The received picture also don't show the complete original package, there is just a section of an opened blister pack with the returned ball inside visible.The identification of the catalog- and lot number was made based on a patient label sticker on a implant sheet.A review of the device history for the reported lot did not indicate any abnormalities.No corrective actions are required at this time.A review of the labeling did not indicate any abnormalities.No indications of material, manufacturing or design related problems were found during the investigation.Based on the available information the root cause of this occurrence cannot be defined and without the original package it is not possible to confirm the event.As part of the complaint evaluation the complete manufacturing process of the device was reviewed.In none of the performed process steps is a steel ball with a similar dimension used.Also the areas with balls, that could get in contact with the product, of the involved machines were reviewed.It was found that none of these balls is missing and that these balls do not have the same diameter like the returned one.These findings speak against a contamination with the ball during the manufacturing and packaging process.If more information is provided, the case will be reassessed.
 
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Brand Name
STANDARD BARREL HIP PLATE, KEYED OMEGA 3 135°, 4 HOLES
Type of Device
APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
Manufacturer (Section D)
STRYKER GMBH
bohnackerweg 1
postfach
selzach 2545
SZ  2545
Manufacturer (Section G)
STRYKER GMBH
bohnackerweg 1
postfach
selzach 2545
SZ   2545
Manufacturer Contact
sharon rivas
325 corporate drive
mahwah, NJ 07430
2018315000
MDR Report Key13524633
MDR Text Key285559495
Report Number0008031020-2022-00054
Device Sequence Number1
Product Code KTT
UDI-Device Identifier07613154325085
UDI-Public07613154325085
Combination Product (y/n)N
Reporter Country CodeUK
PMA/PMN Number
K062066
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Health Professional
Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date 04/28/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/14/2022
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number597024S
Device Catalogue Number597024S
Device Lot NumberH48947
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer02/01/2022
Is the Reporter a Health Professional? Yes
Date Manufacturer Received04/05/2022
Was Device Evaluated by Manufacturer? No
Date Device Manufactured08/27/2021
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
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