MAUDE Adverse Event Report: LDR MÉDICAL MOBI-C IMPLANT "M" STANDARD 15X15 H5 US; MOBI-C CERVICAL DISC PROSTHESIS

Catalog Number	MB3555
Medical Device Problem Code	Migration (4003)
Health Effect - Clinical Code	Pain (1994)
Date of Event	03/01/2022
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Without a product return, no product evaluation is able to be conducted.The lot number is unknown; therefore the device history records are unable to be reviewed.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 a mobi-c device subsided after the patient went on an amusement park ride three months post-operatively.The patient is currently being treated non-operatively for new left shoulder and arm pain.However, a future revision to remove the mobi-c and convert it to an acdf has not been ruled out.
Additional Manufacturer Narrative
Device evaluation: product was not returned and no photos were provided.Product information is not known.A device evaluation, complaint history search and recall search are unable to be performed.Root cause: root cause was unable to be determined.This event could possibly be attributed to riding a roller coaster 3 months post-operatively, as mentioned in the complaint description.Dhr review: dhr review unable to be performed as lot number is not known.Device usage: this device is used for treatment.If additional information is obtained that adds value to the relevant content of this report, a follow-up report will be sent.
Event or Problem Description
It was reported that a mobi-c device subsided after the patient went on an amusement park ride three months post-operatively.The patient is currently being treated non-operatively for new left shoulder and arm pain.However, a future revision to remove the mobi-c and convert it to an acdf has not been ruled out.
Event or Problem Description
It was reported that a mobi-c device subsided at c4/5 after the patient went on an amusement park ride three months post-operatively.The patient was initially treated non-operatively for new left shoulder and arm pain.However, a revision surgery was later performed to remove the mobi-c devices at c3/4 and c4/5 and replace them with competitive product after the device at c3/4 migrated.This is report one of two for this event.
Additional Manufacturer Narrative
Corrections in d4: catalog, lot, and udi numbers.Additional information in d4: expiration date, and h6: health effect.Reference report 3004788213-2023-00013.Current information is insufficient to permit a valid conclusion about the cause of this event.A follow up report will be sent upon completion of the device evaluation.
Additional Manufacturer Narrative
Device evaluation: x-rays were provided which demonstrate the subsidence.The complaint is confirmed.Root cause: root cause was unable to be determined.This event could possibly be attributed to riding a roller coaster 3 months post-operatively, as mentioned in the complaint description.Dhr review: per dhr review, the part was likely conforming when it left zimvie control.Device usage: this device is used for treatment.If additional information is obtained that adds value to the relevant content of this report, a follow-up report will be sent.
Event or Problem Description
It was reported that a mobi-c device subsided at c4/5 after the patient went on an amusement park ride three months post-operatively.The patient was initially treated non-operatively for new left shoulder and arm pain.However, a revision surgery was later performed to remove the mobi-c devices at c3/4 and c4/5 and replace them with competitive product after the device at c3/4 migrated.This is report one of two for this event.

• Brand Name: MOBI-C IMPLANT "M" STANDARD 15X15 H5 US
• Common Device Name: MOBI-C CERVICAL DISC PROSTHESIS
• Manufacturer (Section D): LDR MÉDICAL; quartier europe de l¿ouest; 5, rue de berlin; sainte-savine, na 10300 ; FR 10300
• Manufacturer (Section G): LDR MÉDICAL; quartier europe de l¿ouest; 5, rue de berlin; sainte-savine, na 10300 ; FR 10300
• Manufacturer Contact: kim martinez ; 10225 westmoor dr.; na; westminster, CO 80021 ; 3035144809
• MDR Report Key: 15789281
• Report Number: 3004788213-2022-00094
• Device Sequence Number: 5472275
• Product Code: MJO
• UDI-Device Identifier: 03662663000062
• UDI-Public: (01)03662663000062(17)251201(10)5375655
• Combination Product (Y/N): N
• Initial Reporter State: MD
• Initial Reporter Country: US
• PMA/510(K) Number: P110009
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2023
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Study,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 04/27/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 12/01/2025
• Device Catalogue Number: MB3555
• Device Lot Number: 5375655
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/19/2022
• Supplement Date Received by Manufacturer: 12/20/2022; 01/24/2023; 04/17/2023
• Initial Report FDA Received Date: 11/14/2022
• Supplement Report FDA Received Date: 01/05/2023; 02/17/2023; 04/27/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 01/26/2021
• 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
• Outcome Attributed to Adverse Event: Required Intervention; Other; Hospitalization
• Patient Age: 48 YR
• Patient Sex: Male
• Patient Ethnicity: Non Hispanic
• Patient Race: White