MAUDE Adverse Event Report: ZIMMER BIOMET, INC. TAPERLOC COMPLETE; PROSTHESIS, HIP

Catalog Number	51-103170
Medical Device Problem Code	Manufacturing, Packaging or Shipping Problem (2975)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/11/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).D10: 51-100040 item name tprlc 133 fp type1 pps so 4.0 lot # 6238377.51-104170 item name tprlc 133 t1 pps ho 17x154mm lot # 7220855.51-145170 item name tprlc xr mp t1 pps 17x119mm lot # 7104665.51-107170 item name tprlc 133 mp type1 pps ho 17.0 lot # 7257528.51-107170 item name tprlc 133 mp type1 pps ho 17.0 lot # 7247937.51-106170 item name tprlc 133 mp type1 pps so 17.0 lot # 6639627.51-105170 item name tprlc xr t1 pps 17x154mm lot # 7224452.51-104170 item name tprlc 133 t1 pps ho 17x154mm lot # 6130017.51-104140 item name tprlc 133 t1 pps ho 14x148mm lot # 7114087.51-145140 item name tprlc xr mp t1 pps 14x113mm lot # 6527595.51-104170 item name tprlc 133 t1 pps ho 17x154mm lot # 6924051.51-105140 item name tprlc xr t1 pps 14x148mm lot # 6852411.51-106170 item name tprlc 133 mp type1 pps so 17.0 lot # 6118645.51-104140 item name tprlc 133 t1 pps ho 14x148mm lot # 3938957.51-105160 item name tprlc xr t1 pps 16x152mm lot # 6238851.51-145150 item name tprlc xr mp t1 pps 15x115mm lot # 7281467.G2: foreign: japan.The product has been received by zimmer biomet.The investigation is currently in process.Once the investigation has been completed, a follow-up report will be submitted.
Event or Problem Description
It was reported that while inspecting the product, the sterile packaging was found damaged.There was no patient involvement.There is no further information available at the time of this report.
Additional Manufacturer Narrative
(b)(4) this follow-up report is being submitted to relay additional information.The following sections were updated: g3; h2; h3; h6.The following sections were corrected: d1.Visual evaluation of the returned product/provided photos identified damage to the sterile packaging (blister).Sterility has not been compromised.Review of the device history records identified no deviations or anomalies during manufacturing related to the reported event.The reported event did not occur in an operating room or as part of a medical procedure; medical records are not available for review.The condition of the device when it left zimmer biomet is considered conforming to specification.The root cause of the reported event can be attributed to transit damage and a packaging design issue.The reported event has been confirmed by evaluation of the returned product and provided photos.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
No further information is available at the time of this report.

• Brand Name: TAPERLOC COMPLETE
• Common Device Name: PROSTHESIS, HIP
• 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: 21949883
• Report Number: 0001825034-2025-01309
• Device Sequence Number: 12961723
• Product Code: LZO
• UDI-Device Identifier: 00880304498341
• UDI-Public: (01)00880304498341(17)251222(10)3697093
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: K200196
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Company Representative,Distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 09/03/2025

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 Expiration Date: 12/22/2025
• Device Catalogue Number: 51-103170
• Device Lot Number: 3697093
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 04/28/2025
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/11/2025
• Supplement Date Received by Manufacturer: 08/13/2025
• Initial Report FDA Received Date: 05/02/2025
• Supplement Report FDA Received Date: 09/03/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 12/22/2015
• 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
• Concomitant Medical Products and Therapy/Usage Dates: PLEASE SEE H11
• Patient Sex: Unknown