ZIMMER SWITZERLAND MANFACTURING GMBH BLUNT TIP SCREW, 4X42MM; AFFIXUS(R) NATURAL NAIL(R) SYSTEM HUMERAL NAIL
|
Back to Search Results |
|
Model Number N/A |
Device Problems
Migration or Expulsion of Device (1395); Patient Device Interaction Problem (4001)
|
Patient Problems
Insufficient Information (4580); No Clinical Signs, Symptoms or Conditions (4582)
|
Event Date 02/24/2022 |
Event Type
Injury
|
Event Description
|
It was reported that: operation was performed with ann nail.After 4 days from the initial, surgeon found #2 screw of the proximal screws was backed out from the proper position.The surgeon keep an eye on the patient condition as well as no revision will be planned so far.Patient outcome - migration.
|
|
Manufacturer Narrative
|
Medical product: proximal humerus, left, 11x160mm, catalog#: 47-2496-161-11 ; lot#: 3051303.Blunt tip screw, 4x42mm, catalog#: 47-2486-042-40; lot#: 3039349.Cortical bone screw, 4x28mm, catalog#: 47-2486-128-40; lot#: 3076797.Proximal humerus nail cap, 0mm, catalog#: 47-2488-010-00; lot#: 3076775.Cortical bone screw, 4x30mm, catalog#: 47-2486-130-40; lot#: 3073753.The manufacturer did not receive x-rays, or other source documents for review.The manufacturer did not receive the device for investigation.The lot number of the device was received.The device history records will be reviewed during investigation.A cause for this specific event cannot be ascertained from the information provided.As soon as supplemental information becomes available an updated report will be submitted.Zimmer biomet¿s reference number of this file is (b)(4).The following reports are associated with this event: 0009613350-2022-00204; 0009613350-2022-00201.
|
|
Event Description
|
No change to previously reported event.
|
|
Manufacturer Narrative
|
This follow-up report is being submitted to relay additional and/or corrected information.Event description: it was reported, that: operation was performed with ann nail on (b)(6) 2022.After 4 days from the initial, surgeon found #2 screw of the proximal screws was backed out from the proper position.The surgeon keep an eye on the patient condition as well as no revision will be planned so far.Patient outcome: migration.No delay.Review of received data: - no medical records available - due diligence: no further due diligence required as all required information to support the conclusion is available or was already requested.Product evaluation: - no product was returned; therefore, visual and dimensional evaluation could not be performed.Review of product documentation: - device purpose: all involved devices are intended for treatment.- product compatibility: the product combination was approved by zimmer biomet.- surgical technique sap: the surgical technique explains that the locking of the corelock is done using the corelock driver with torque limiting handle.Turn slowly clockwise to tighten and engage the corelock mechanism until a click is felt from the torque limiting handle.- a complaint history was run which identified additional complaints for the same product and lot number.Conclusion: it was reported, that: operation was performed with ann nail on (b)(6) 2022.After 4 days from the initial, surgeon found #2 screw of the proximal screws was backed out from the proper position.The surgeon keep an eye on the patient condition as well as no revision will be planned so far.Patient outcome: migration.No delay.The quality records show that all specified characteristics have met the specifications valid at the time of production.Based on the investigation it could be assumed that further possible contributing factors to the migration of the screw might be multifactorial related to either patient condition, behaviour or implantation procedure.If and to what extent any of these aspects may have influenced the migration of the screw remains unknown.An additional deeper investigation was performed which identified the design limitation of the corelock mechanism as a potential contributing factor.However, as further biomechanical testing was carried out and the performance is in an acceptable range in comparison with legally marketed similar devices, no design changes were conducted.In conclusion, as the cause may be multifactorial an exact root cause could not be identified for the migration of the screw.The need for corrective measures is not indicated and zimmer switzerland manufacturing gmbh considers this case as closed.Zimmer biomet¿s reference number of this file is (b)(4).
|
|
Search Alerts/Recalls
|
|
|