|
|
| Model Number |
628535S |
| Medical Device Problem Codes |
Break (1069); Positioning Failure (1158)
|
| Health Effect - Clinical Code |
No Clinical Signs, Symptoms or Conditions (4582)
|
| Date of Event |
09/04/2020
|
|
Type of Reportable Event
|
Malfunction
|
|
Additional Manufacturer Narrative
|
|
Device will not be returned.If additional information becomes available, it will be provided in a supplemental report.
|
| |
|
Event or Problem Description
|
|
As reported: "[event details] when the clavicle hook plate was operated, the locking screw did not lock in the locking hole.Plate used: 628535s location of defective lock: front side of the plate's most distal hole occurrence status: insert 3 screws after setting the plate ((1) elliptical hole: non-locking, (2) round hole next to the ellipse distal side: rocking, (4) far-most rear circular hole: rocking).A phenomenon that the locking screw does not lock when the locking screw is inserted 18mm into the 4th most distal locking hole.Set it there and insert the locking screw into the most recent hole (lock without any problem).I tried the following for holes that did not lock again.Check the drilling direction no problem (the guide sleeve was within the swing range).Confirmation of plate lip and screw head no interstitial tissue such as soft tissue can be confirmed on the lip.As far as i could see the screw head, it seemed to be no problem.Change the drill direction and insert another locking screw 16 mm again, but it does not lock.Finally, at the discretion of dr., it ends without inserting a screw into the hole." "the plate is currently inside the patient's body." additional information from sales rep: i don't know when it happened, but i think that the lip of the plate has broken.There was nothing wrong with dr's movements during drilling and insertion, and he did the same as in the other holes, so the cause is unknown.For patients, it has been confirmed that there is no problem with immobility by confirming the range of motion after immobilization, and it is considered that there is currently no health hazard or adverse event.
|
| |
|
Event or Problem Description
|
|
As reported: "[event details] when the clavicle hook plate was operated, the locking screw did not lock in the locking hole.Plate used: 628535s location of defective lock: front side of the plate's most distal hole occurrence status: - insert 3 screws after setting the plate ((1) elliptical hole: non-locking, (2) round hole next to the ellipse distal side: rocking, (4) far-most rear circular hole: rocking) - a phenomenon that the locking screw does not lock when the locking screw is inserted 18mm into the 4th most distal locking hole - set it there and insert the locking screw into the most recent hole (lock without any problem) - i tried the following for holes that did not lock again - check the drilling direction ¿ no problem (the guide sleeve was within the swing range) - confirmation of plate lip and screw head ¿ no interstitial tissue such as soft tissue can be confirmed on the lip.As far as i could see the screw head, it seemed to be no problem.- change the drill direction and insert another locking screw 16 mm again, but it does not lock - finally, at the discretion of dr., it ends without inserting a screw into the hole." "the plate is currently inside the patient's body [.]." additional information from sales rep: - i don't know when it happened, but i think that the lip of the plate has broken.- there was nothing wrong with dr's movements during drilling and insertion, and he did the same as in the other holes, so the cause is unknown.- for patients, it has been confirmed that there is no problem with immobility by confirming the range of motion after immobilization, and it is considered that there is currently no health hazard or adverse event.
|
| |
|
Additional Manufacturer Narrative
|
|
The reported event could not be confirmed, since the device was not returned for evaluation and no other evidences were provided.More detailed information about the complaint event as well as the affected device must be available in order to determine the root cause of the complaint event.A nonconformance report has been opened in order to further investigate and address this issue for further details.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.If the device is returned or if any additional information is provided, the investigation will be reassessed.
|
| |
|
Search Alerts/Recalls
|
|
|