MAUDE Adverse Event Report: ZIMMER BIOMET, INC. EXPLOR 14X24 MM IMPLANT HEAD; EXTREMITY IMPLANT

Model Number	N/A
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Failure of Implant (1924); Pain (1994)
Date of Event	08/19/2015
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).D10 - medical product: catalog #: 11-210064, explor 9x30mm impl stem w/scr, lot # 947750.G2: norway.H3: customer has indicated that the product will not be returned to zimmer biomet for investigation, as the device has been discarded.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.
Event or Problem Description
It was reported that the patient experienced pain and crepitation in elbow at approximately 2.5 years post op.Radiology showed loosening of the stem and the patient was revised.Attempts have been made and there is no further information at this time.
Additional Manufacturer Narrative
(b)(4).Updated: b4, b5, d2, d4 (exp date), d6a, g3, h1, h2, h4, h11.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.
Event or Problem Description
It was further reported that the initial surgery was performed approximately 11 years ago.
Event or Problem Description
Voiding the radial head as the pain is related to the loosening of humeral stem and not with the articulation of the humeral head.
Additional Manufacturer Narrative
(b)(4).Proposed g-code: mechanical (g04) - head.Voiding the radial head as the pain is related to the loosening of humeral stem and not with the articulation of the humeral head.Reported event was unable to be confirmed due to limited information received from the customer.Device history record was reviewed and no discrepancies relevant to the reported event were found.A definitive root cause could not be determined.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.

• Brand Name: EXPLOR 14X24 MM IMPLANT HEAD
• Common Device Name: EXTREMITY IMPLANT
• Manufacturer (Section D): ZIMMER BIOMET, INC.; 56 e. bell drive; p.o. box 587; warsaw IN 46581
• Manufacturer (Section G): ZIMMER BIOMET, INC.; 56 e. bell drive; p.o. box 587; warsaw IN 46581
• Manufacturer Contact: jennifer rapsavage ; 56 e. bell dr.; warsaw, IN 46582 ; 5745260384
• MDR Report Key: 19654734
• Report Number: 0001825034-2024-01736
• Device Sequence Number: 6624403
• Product Code: KWI
• UDI-Device Identifier: 00880304438330
• UDI-Public: (01)00880304438330(17)210930(10)572570
• Combination Product (Y/N): N
• Initial Reporter Country: NO
• PMA/510(K) Number: K051385
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2013
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 11/27/2024

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: 09/30/2021
• Device Model Number: N/A
• Device Catalogue Number: 11-210043
• Device Lot Number: 572570
• Was Device Available for Evaluation?: No
• 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: 06/19/2024
• Supplement Date Received by Manufacturer: 07/15/2024; 11/20/2024
• Initial Report FDA Received Date: 07/02/2024
• Supplement Report FDA Received Date: 08/12/2024; 11/27/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 10/04/2011
• 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: Hospitalization; Required Intervention
• Patient Sex: Unknown