MAUDE Adverse Event Report: LDR MEDICAL ROI-A MEDIAN IMPLANT PXL : 30X33 H 12MM 10 DEG.; ROI-A ALIF CAGE SYSTEM

Catalog Number	IR2632P
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	10/16/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Without a product return, no product evaluation is able to be conducted.Current information is insufficient to permit a valid conclusion about the cause of this event.If additional information is obtained that adds value to the relevant content of this report and/or a conclusion can be drawn, a follow-up report will be sent.
Event or Problem Description
It was reported that an roi-a cage broke while the anchoring plate was being impacted through it intra-operatively.The anchoring plate was also damaged and could not be used.The surgeon did use the awl to prepare the patient's bone prior to installing the anchoring plate.The cage and plate were removed and replaced with another cage of a different size and another plate to complete the surgery.There were no reported patient impacts.This is report one of two for this event.
Additional Manufacturer Narrative
Corrections in d9 and h3.Additional information h6: component, investigation type, findings, and conclusions.Inspection: the returned device matches the information in the complaint file and was examined.Visual inspection revealed the cage is fractured.Dhr review: the dhr was reviewed.There are no indications of manufacturing issues which would have contributed to this event and the device was likely conforming when it left highridge¿s control.Potential root cause: a definitive root cause cannot be determined with the information provided.This event could possibly be attributed to excessive force applied during surgery.Device usage: this device is used for treatment.A follow-up report will be sent if additional information is obtained that adds value to the relevant content of this report.Reference report 3004788213-2023-00116.
Event or Problem Description
It was reported that an roi-a cage broke while the anchoring plate was being impacted through it intra-operatively.The anchoring plate was also damaged and could not be used.The surgeon did use the awl to prepare the patient's bone prior to installing the anchoring plate.The cage and plate were removed and replaced with another cage of a different size and another plate to complete the surgery.There were no reported patient impacts.This is report one of two for this event.

• Brand Name: ROI-A MEDIAN IMPLANT PXL : 30X33 H 12MM 10 DEG.
• Common Device Name: ROI-A ALIF CAGE SYSTEM
• Manufacturer (Section D): LDR MEDICAL; 5 rue de berlin; quartier europe de l'ouest; sainte-savine 10300 ; FR 10300
• Manufacturer (Section G): LDR MEDICAL; 5 rue de berlin; quartier europe de l'ouest; sainte-savine 10300 ; FR 10300
• Manufacturer Contact: sabrina abla ; 10225 westmoor dr.; westminster, CO 80021 ; 7206965158
• MDR Report Key: 18111768
• Report Number: 3004788213-2023-00115
• Device Sequence Number: 7624388
• Product Code: MAX
• UDI-Device Identifier: 03662663011648
• UDI-Public: (01)03662663011648(17)270601(10)L222822
• Combination Product (Y/N): N
• Initial Reporter Country: FR
• PMA/510(K) Number: K153495
• Exemption Number: 5645646
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 06/06/2024

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: IR2632P
• Device Lot Number: L222822
• 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: Not provided
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 11/10/2023
• Supplement Report FDA Received Date: 06/07/2024
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 06/28/2022
• 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: 43 YR
• Patient Sex: Female
• Patient Weight: 26 KG
• Patient Ethnicity: Non Hispanic