MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US PINN CAN BONE SCREW 6.5MMX50MM; BONE SCREWS AND PINS : SCREWS

Model Number	1217-50-500
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Hemorrhage/Blood Loss/Bleeding (1888); Unspecified Infection (1930); Pain (1994); No Code Available (3191)
Date of Event	04/15/2014
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Initial reporter occupation: lawyer.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
Medical records received.After review of the medical records the patient was revised to address infection, osteomyelitis and pain.Operative note reported 20 ml serous fluid and fibrous tissues.Doi: (b)(6) 2013.Dor: (b)(6) 2014; right hip (2nd revision).
Additional Manufacturer Narrative
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.None of the photos attached depict the reported product.The investigation could not verify or draw any conclusions about the root cause of the reported event without the device to examine.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 (mre) was not performed.

• Brand Name: PINN CAN BONE SCREW 6.5MMX50MM
• Common Device Name: BONE SCREWS AND PINS : SCREWS
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• Manufacturer (Section G): JTE RAYNHAM MFG SITE; 325 paramount drive; raynham MA 02767
• Manufacturer Contact: kara ditty-bovard ; 700 orthopaedic dr.; warsaw, IN 46581-0988 ; 6107428552
• MDR Report Key: 10636319
• Report Number: 1818910-2020-21634
• Device Sequence Number: 3650084
• Product Code: LPH
• UDI-Device Identifier: 10603295010418
• UDI-Public: 10603295010418
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K983014
• 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: Other
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 09/21/2020

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?: No
• Operator of Device: Health Professional
• Device Model Number: 1217-50-500
• Device Catalogue Number: 121750500
• Device Lot Number: YN4JN1000
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Received by Manufacturer: 09/21/2020
• Supplement Date Received by Manufacturer: 09/21/2020; 02/24/2023
• Initial Report FDA Received Date: 10/06/2020
• Supplement Report FDA Received Date: 10/09/2020; 02/27/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 09/21/2011
• 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
• Concomitant Medical Products and Therapy/Usage Dates: PIN LNR CONS NEUT +4 36IDX58OD; PINN CAN BONE SCREW 6.5MMX20MM; PINN CAN BONE SCREW 6.5MMX25MM; PINN MULTIHOLE W/GRIPTION 58MM; STRYKER STANDARD PROXIMAL FEMUR; UNKNOWN BONE CEMENT; UNKNOWN HIP ACETABULAR CUP; UNKNOWN HIP CONSTRAINED ACETABULAR LINERS; UNKNOWN HIP FEMORAL HEAD (STRYKER); UNKNOWN HIP FEMORAL HEAD (STRYKER); UNKNOWN HIP FEMORAL STEM (STRYKER); UNKNOWN HIP IMPLANT (SCREW); UNKNOWN HIP IMPLANT (SCREW); UNKNOWN HIP IMPLANT (SCREW); UNKNOWN HIP ACETABULAR CUP; UNKNOWN HIP CONSTRAINED ACETABULAR LINERS; UNKNOWN HIP FEMORAL HEAD (STRYKER); UNKNOWN HIP FEMORAL STEM (STRYKER); UNKNOWN HIP IMPLANT (SCREW); UNKNOWN HIP IMPLANT (SCREW); UNKNOWN HIP IMPLANT (SCREW)
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 69 YR
• Patient Sex: Female
• Patient Ethnicity: Non Hispanic
• Patient Race: White