MAUDE Adverse Event Report: STRYKER GMBH TRANSPORT STRUT HOFFMANN LRF; APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

Model Number	4933-0-400
Medical Device Problem Codes	Break (1069); Fracture (1260)
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	08/02/2022
Type of Reportable Event	Malfunction
Event or Problem Description
As reported: "patient came in and one of the struts was not transporting making the transporting bone shift and not line up to docking site.Patient had to spend an extra hour as the surgeon had replace the broken strut in clinic.This may delay his docking procedure in the future".
Additional Manufacturer Narrative
Once the investigation has been completed any additional information will be reported in a supplemental report.
Event or Problem Description
As reported: "patient came in and one of the struts was not transporting making the transporting bone shift and not line up to docking site.Patient had to spend an extra hour as the surgeon had replace the broken strut in clinic.This may delay his docking procedure in the future".
Additional Manufacturer Narrative
The complaint could be confirmed, since the product was returned for evaluation and matches the alleged failure.Visual evaluation: the optical and functional evaluation of the returned part shows that the part got returned in a used condition and it got found that the part is not functional on the lower end.Dimensional inspection: the returned part got through dimensional inspection by production, the part meats all measurements.Inspection of the received information/evidences are done or will be done, in the proceedings of the nc.If more information is provided, the case will be reassessed.
Event or Problem Description
As reported: "patient came in and one of the struts was not transporting making the transporting bone shift and not line up to docking site.Patient had to spend an extra hour as the surgeon had replace the broken strut in clinic.This may delay his docking procedure in the future".
Additional Manufacturer Narrative
Recall number added to h9.
Additional Manufacturer Narrative
The complaint could be confirmed, since the product was returned for evaluation and matches the alleged failure.Visual evaluation: the optical and functional evaluation of the returned part shows that the part got returned in a used condition and it got found that the part is not functional on the lower end.Dimensional inspection: the returned part got through dimensional inspection by production, the part meats all measurements.Inspection of the received information/evidences are done or will be done, in the proceedings of the nc.R&d has done first inspection and reviewed the received information and noted: there were samples which showed ¿deformations¿ which can be caused by one non-functioning strut in the frame construct.If more information is provided, the case will be reassessed.
Event or Problem Description
As reported: "patient came in and one of the struts was not transporting making the transporting bone shift and not line up to docking site.Patient had to spend an extra hour as the surgeon had replace the broken strut in clinic.This may delay his docking procedure in the future".

• Brand Name: TRANSPORT STRUT HOFFMANN LRF
• Common Device Name: 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: anna jusinski ; 325 corporate drive; mahwah, NJ 07430 ; 2018315000
• MDR Report Key: 15298912
• Report Number: 0008031020-2022-00414
• Device Sequence Number: 17915290
• Product Code: KTT
• UDI-Device Identifier: 07613327094640
• UDI-Public: 07613327094640
• Combination Product (Y/N): N
• Initial Reporter State: GA
• Initial Reporter Country: US
• PMA/510(K) Number: K153377
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2022
• Device Explanted Year: 2022
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Physician
• Remedial Action: Recall
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 05/23/2023

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: Lay User/Patient
• Device Model Number: 4933-0-400
• Device Catalogue Number: 49330400
• Device Lot Number: D40690
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 08/02/2022
• Supplement Date Received by Manufacturer: 10/26/2022; 04/17/2023; 04/26/2023
• Initial Report FDA Received Date: 08/25/2022
• Supplement Report FDA Received Date: 11/22/2022; 04/17/2023; 05/23/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 07/19/2019
• 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
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: 3152674
• Patient Sequence Number: 1
• Patient Age: 35 YR
• Patient Sex: Male
• Patient Weight: 100 KG