MAUDE Adverse Event Report: SMITH & NEPHEW, INC. R3 36MM ID US CRMC LINER 52MM; PROSTHESIS, HIP, HEMI-, TRUNNION-BEARING, FEMORAL, METAL/POLYACETAL

Catalog Number	71338952
Medical Device Problem Code	Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	Pain (1994)
Date of Event	08/27/2018
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that revision surgery was performed.Surgeon revised r3 alumina on alumina.Patient was complaining of pain, thought ceramic liner might be fractured.It was found that the ceramic liner was not fractured, implants were fine.Surgeon changed liner to a poly liner and a new femoral head was put on.No issues, no delays, no injuries.
Additional Manufacturer Narrative
The associated complaint device was not returned for evaluation.A review of complaint history for the listed part revealed no prior complaints for the listed batch.A review of the manufacturing or product specifications for listed batch did not reveal abnormalities that could have contributed to the reported issue.Our clinical/medical team concluded that no relevant supporting clinical information has been provided to assist with a clinical investigation, and the patient's current condition is unknown.Therefore based on insufficient information, a thorough clinical assessment cannot be performed at this time.Without the actual product involved, our investigation cannot proceed.If the device or new information is received in the future, this complaint can be re-opened.No further actions are being taken at this time.We consider this investigation closed.

• Brand Name: R3 36MM ID US CRMC LINER 52MM
• Common Device Name: PROSTHESIS, HIP, HEMI-, TRUNNION-BEARING, FEMORAL, METAL/POLYACETAL
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 1450 brooks road; memphis TN 38116
• MDR Report Key: 7899528
• Report Number: 1020279-2018-01855
• Device Sequence Number: 1586235
• Product Code: JDH
• UDI-Device Identifier: 00885556021552
• UDI-Public: 00885556021552
• Combination Product (Y/N): N
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 12/27/2018

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 Catalogue Number: 71338952
• Device Lot Number: 09FT33137
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 08/27/2018
• Supplement Date Received by Manufacturer: 08/27/2018
• Initial Report FDA Received Date: 09/21/2018
• Supplement Report FDA Received Date: 12/27/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Age: 58 YR