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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STRYKER TRAUMA KIEL TROCHANTERIC NAIL KIT, STST GAMMA3® Ø11X180MM X 125°; ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

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STRYKER TRAUMA KIEL TROCHANTERIC NAIL KIT, STST GAMMA3® Ø11X180MM X 125°; ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES Back to Search Results
Catalog Number 41251180S
Device Problems Entrapment of Device (1212); Difficult to Remove (1528)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 10/11/2019
Event Type  malfunction  
Manufacturer Narrative
Once the investigation has been completed any additional information will be reported in a supplemental report.
 
Event Description
At the time the surgeon was going to implant the gamma nail, the arch became trapped in the nail entry thread.At the time the surgeon tried to remove the arch, it had to be removed with the implant included.Additionally, it was necessary to remove all screws that were place into the patient.To finished the surgery it was necessary to open a new implant and the patient had to receive double anesthesia for the operative time.
 
Manufacturer Narrative
The reported event could be confirmed.The device inspection revealed the following: the devices namely target device, nail and nail holding screw were received in a stuck state.After inspecting the overall appearance, it was observed that the target device was severely damaged around the head region possibly with a sharp tool during the surgery (however not related with the current event).The nail holding screw was stuck inside the target device with its distal part firmly attached to the nail.One of its side was dented, which possibly would have been caused in an attempt to disassemble it initially.The nail appeared free from any visible damage.A functional inspection could not be performed (without deforming them) as the devices were firmly stuck together.Without dis-assembling the devices it is not possible to determine the exact root cause of the failure.This is the first reported case with this lot number.A review of the labeling did not indicate any abnormalities.If any further information is provided, the complaint report will be updated.
 
Event Description
At the time the surgeon was going to implant the gamma nail, the arch became trapped in the nail entry thread.At the time the surgeon tried to remove the arch, it had to be removed with the implant included.Additionally, it was necessary to remove all screws that were place into the patient.To finished the surgery it was necessary to open a new implant and the patient had to receive double anesthesia for the operative time.
 
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Brand Name
TROCHANTERIC NAIL KIT, STST GAMMA3® Ø11X180MM X 125°
Type of Device
ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES
Manufacturer (Section D)
STRYKER TRAUMA KIEL
prof. kuentscher-strasse 1-5
schoenkirchen/kiel D-242 32
DE  D-24232
MDR Report Key9319339
MDR Text Key191823652
Report Number0009610622-2019-00920
Device Sequence Number1
Product Code HSB
Combination Product (y/n)N
PMA/PMN Number
K043431
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,other
Type of Report Initial,Followup
Report Date 01/22/2020
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 Catalogue Number41251180S
Device Lot NumberKU110654
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer11/26/2019
Initial Date Manufacturer Received 10/16/2019
Initial Date FDA Received11/13/2019
Supplement Dates Manufacturer Received12/24/2019
Supplement Dates FDA Received01/22/2020
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
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