MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US SROM*NRH REPL HINGE PIN/XSM/SM; BONE SCREWS AND PINS : KNEE TIBIAL INSERT ACCESSORY

Model Number	62-1640
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	12/28/2022
Type of Reportable Event	Serious Injury
Event or Problem Description
The first surgery was on the (b)(6) 2022, after sterilizing the material removing the inner boxes, the trays and putting everything wrapped in paper and all the sterile material came out, but today dr.(b)(6) (the surgeon), has returned to the patient, because the wound stained and they suspect that it is infected, for that reason they have put it today to open the wound and wash it abundantly to see if you can avoid having to remove all the material.As i told you, the surgery of day 7th, was a replacement of a ptr that had eaten polyethylene and was touching metal / metal, which had caused an enormous metallosis in the joint, during the surgery the knee prosthesis that had the patient was removed, metallosis was removed and our noiles knee replacement prosthesis was implanted.At that time there were no markers of any possible infection.Today, after taking samples, washing the wound and cleaning it, we proceeded to change the polyethylene and the pin, the rest of the components were maintained.Did the patient experience an adverse event such as infection, non-union, allergic reaction, osteoporosis, overloading, pain, degenerative diseases, bleeding or oozing? unknown, did the patient require revision surgery or hardware removal? unknown, patient status/ outcome / consequences, was other medical intervention (e.G.X-rays, additional procedures, prescriptions, otc, revision) required: unknown, is the patient part of a clinical study : unknown, (b)(4).Device property of none, device in possession of none, (b)(4).Device property of none, device in possession of none, (b)(4) device property of none, device in possession of none, (b)(4).Be submitted through cst.True.
Additional Manufacturer Narrative
Product complaint # (b)(4).Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Event or Problem Description
Additional information received indicated that the components that were frightened were those of the second intervention, the poly and the bolt, when an infected ptr was washed/cleaned, it was usual to change the polyethylene, the rest were left until it wass verified that the infection did not go away and everything had to be removed.There was no loosening.Affected side was left knee.
Additional Manufacturer Narrative
Product complaint # (b)(4).This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information which has not been investigated or verified prior to the required reporting date.This report does not reflect a conclusion by depuy synthes joint reconstruction, or its employees that the report constitutes an admission that the product, depuy synthes joint reconstruction, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.
Additional Manufacturer Narrative
Product complaint # (b)(4).Investigation summary: no device associated with this report was received for examination.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.Device history lot: the product investigation found no evidence suspecting an error in the manufacturing or material that would be a contributing factor in the reported allegation(s).A manufacturing records evaluation (mre) was not performed.

• Common Device Name: BONE SCREWS AND PINS : KNEE TIBIAL INSERT ACCESSORY
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• Manufacturer (Section G): DEPUY RAYNHAM, A DIV. OF DEPUY ORTHO 1219655; 325 paramount drive; raynham MA 02767
• Manufacturer Contact: kate karberg ; 700 orthpaedic dr.; warsaw, IN 46581 ; 3035526892
• MDR Report Key: 16131799
• Report Number: 1818910-2023-00914
• Device Sequence Number: 7654987
• Product Code: JWH
• UDI-Device Identifier: 10603295179108
• UDI-Public: 10603295179108
• Combination Product (Y/N): N
• Initial Reporter Country: SP
• PMA/510(K) Number: K870730
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2022
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 01/10/2023

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?: No
• Operator of Device: Health Professional
• Device Model Number: 62-1640
• Device Catalogue Number: 621640
• Device Lot Number: HJ2613
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/27/2022
• Supplement Date Received by Manufacturer: 02/09/2023; 02/23/2023
• Initial Report FDA Received Date: 01/10/2023
• Supplement Report FDA Received Date: 02/13/2023; 02/23/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 10/26/2017
• 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: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: LPS UNIV TIB HIN INS SM 16MM.; MBT TRAY SLEEVE POR M/L 37MM.; UNIVERSAL STEM 115X12MM FLUTED.
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown