MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US P.F.C.*LINR 48-52/10 DEG-28MM; PFC HIP STEM AND LINER IMPLANTS : HIP POLY ACETABULAR LINERS

Model Number	85-7723
Medical Device Problem Codes	Naturally Worn (2988); Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Pain (1994); No Code Available (3191)
Date of Event	02/07/2020
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).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
It was reported that a (b)(6) year old patient complains of pain in hip so the surgeon brought patient in for poly swap.No components were lose or damaged.Head was removed.After many minutes the poly liner was removed, the aid of osteotomes and other instruments was needed to remove the existing poly.Once removed the poly was damaged and sizes were not recognizable.Trials were not available due to emergent status of the procedure.An approximate sized implant was opened and was incorrect.We then opened the correct size and implanted successfully.A replacement head was opened and procedure was complete.Doi: unknown.Dor: (b)(6) 2020, unknown affected side.
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.  h6: the previous device code (implant bearing wear - polyethylene) is being retracted because it was further identified that there was no wear.
Additional Manufacturer Narrative
Depuy synthes is submitting this report pursuant to the provision of 21 cfr, part 803.The report may be based on the 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.H10 additional narrative: corrected:h6(device codes).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.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

• Common Device Name: PFC HIP STEM AND LINER IMPLANTS : HIP POLY ACETABULAR LINERS
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 9745903
• Report Number: 1818910-2020-05766
• Device Sequence Number: 1974044
• Product Code: JDI
• UDI-Device Identifier: 10603295215196
• UDI-Public: 10603295215196
• Combination Product (Y/N): N
• Initial Reporter State: CO
• Initial Reporter Country: US
• PMA/510(K) Number: K873585
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Explanted Year: 2020
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 02/07/2020

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 Model Number: 85-7723
• Device Catalogue Number: 857723
• Device Lot Number: 8403157
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 02/07/2020
• Supplement Date Received by Manufacturer: 02/20/2020; 03/27/2020
• Initial Report FDA Received Date: 02/24/2020
• Supplement Report FDA Received Date: 03/06/2020; 03/30/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: P.F.C.*LINR 48-52/10 DEG-28MM; UNKNOWN HIP FEMORAL HEAD; P.F.C.*LINR 48-52/ 10 DEG-28MM; UNKNOWN HIP FEMORAL HEAD
• Outcome Attributed to Adverse Event: Required Intervention