MAUDE Adverse Event Report: STRYKER GMBH INTERMEDIATE NAIL, LEFT GAMMA4 Ø10X240MM X 125°; ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

Catalog Number	83250240S
Medical Device Problem Code	Device Damaged by Another Device (2915)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/04/2024
Type of Reportable Event	Malfunction
Event or Problem Description
As reported: "g4 intermediate nail miss drill was occurred on lateral side during drilling of distal dynamic hole.Pre-calibration showed correct targeting.The cortical bone and nail were in contact at the lateral end, and the physician determined that the miss drill was due to loading on the nail.".
Additional Manufacturer Narrative
Based on the available information the device will not be returned therefore an evaluation of the device cannot be performed.Should additional information become available, it will be provided in a supplemental report.H3 other text : device remains implanted in the patient.
Additional Manufacturer Narrative
Please note corrections to: d1 / product long description, d4 / catalog#, d4 / gtin#, g4 / 510k# the reported event could not be confirmed since the device was not returned for evaluation and no other evidences was provided.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 did the affected devices pass the intra-operative function test before insertion and also the post-operative function test as the instruments are continued to be used.Therefore, a product related issue can be excluded and the event was most likely use related, which is also indicated by statement in the event description that there was possibly to much load on the nail.If more information is provided, the case will be reassessed.
Event or Problem Description
As reported: "g4 intermediate nail miss drill was occurred on lateral side during drilling of distal dynamic hole.Pre-calibration showed correct targeting.The cortical bone and nail were in contact at the lateral end, and the physician determined that the miss drill was due to loading on the nail.".

• Brand Name: INTERMEDIATE NAIL, LEFT GAMMA4 Ø10X240MM X 125°
• Common Device Name: ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES
• Manufacturer (Section D): STRYKER GMBH; bohnackerweg 1; postfach; selzach 2545 ; SZ 2545
• Manufacturer (Section G): STRYKER TRAUMA KIEL; prof. kuentscher-strasse 1-5; schoenkirchen/kiel D-242 32; GM D-24232
• Manufacturer Contact: anna jusinski ; 325 corporate drive; mahwah, NJ 07430 ; 2018315000
• MDR Report Key: 18620127
• Report Number: 0009610622-2024-00049
• Device Sequence Number: 7576281
• Product Code: HSB
• UDI-Device Identifier: 07613327593877
• UDI-Public: 07613327593877
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: K230512
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 04/04/2024

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 Catalogue Number: 83250240S
• Device Lot Number: K1776E5
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 01/04/2024
• Supplement Date Received by Manufacturer: 03/06/2024
• Initial Report FDA Received Date: 01/31/2024
• Supplement Report FDA Received Date: 04/04/2024
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 09/28/2023
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Age: 89 YR
• Patient Sex: Female
• Patient Weight: 50 KG