MAUDE Adverse Event Report: ZIMMER DENTAL IMP, TSV, 3.7, 10,MTX,MC,MG,HA; DENTAL IMPLANT

Model Number	TSVMH10
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	Insufficient Information (4580)
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that the implant was removed due to becoming fractured at the site.
Additional Manufacturer Narrative
Zimmer biomet complaint number (b)(4).Patient weight not provided.Event date not provided.
Additional Manufacturer Narrative
Zimvie complaint number (b)(4).An implant was returned for investigation.Visual inspection of the as returned product identified worn marking due to usage, bone and a fracture at the collar.Also, an associated product hc343 has not been returned.However, this item is listed as associated item only and did not cause or contribute to the event.No further investigation will be conducted.No pre-existing conditions were noted on the per.The reported device was location is 18 and was used for approximately 6 years.Pictures or x-ray images were not provided.Review of appropriate documentation: instructions for use for tapered screw-vent® and trabecular metal¿ implants ifu 4869 rev 9 ¿ 10/19 information identified: 'contraindications' 'warnings' 'changes in performance' 'adverse effects' dhr review: dhr review was completed for the subject lot number (63802111).It was confirmed that all operations and inspections were executed as per applicable procedure.No deviations or non-conformances, which could have caused or contributed to the reported event was noted as part of the dhr.Lot was inspected and passed all acceptance criteria by qa.Complaint history review: complaint history review was performed for the reported lot number (63802111) for similar event and no other complaint was identified.Post market trend review: nov post market trending was reviewed and there were no actionable events or corrective actions for the reported event or device.Based on the available information, device malfunction did occur and the reported event was confirmed.
Event or Problem Description
No further event information is available at the time of this report.

• Brand Name: IMP, TSV, 3.7, 10,MTX,MC,MG,HA
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): ZIMMER DENTAL; 4555 riverside drive; palm beach gardens FL 33410
• Manufacturer (Section G): ZIMMER DENTAL; 4555 riverside drive; palm beach gardens FL 33410
• Manufacturer Contact: susanne taylor ; 4555 riverside drive; palm beach gardens, FL 33410 ; 5617766700
• MDR Report Key: 15257536
• Report Number: 0002023141-2022-02111
• Device Sequence Number: 14905710
• Product Code: DZE
• UDI-Device Identifier: 00889024344099
• UDI-Public: (01)00889024344099(10)63802111(17)221031
• Combination Product (Y/N): N
• Initial Reporter Country: GM
• PMA/510(K) Number: K133339
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional
• Initial Reporter Occupation: Dentist
• Type of Report: Initial,Followup
• Report Date (Section B): 01/31/2023

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: Lay User/Patient
• Device Expiration Date: 10/31/2022
• Device Model Number: TSVMH10
• Device Catalogue Number: TSVMH10
• Device Lot Number: 63802111
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/08/2022
• 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: 08/08/2022
• Supplement Date Received by Manufacturer: 01/17/2023
• Initial Report FDA Received Date: 08/19/2022
• Supplement Report FDA Received Date: 01/31/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 10/09/2017
• 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: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 70 YR
• Patient Sex: Female