MAUDE Adverse Event Report: SMITH & NEPHEW, INC. OXINIUM FEM HD 12/14 22 MM +8; PRSTHSIS, HIP, SEMCNSTRIND, MTALCRAMICPLYMR CMNTD R NN-POROUS, NCMNTD

Catalog Number	71342208
Medical Device Problem Code	Device Dislodged or Dislocated (2923)
Health Effect - Clinical Code	Joint Dislocation (2374)
Date of Event	11/27/2017
Type of Reportable Event	Serious Injury
Event or Problem Description
Patient was putting on clothes and dislocated.This was originally put in (b)(6) 2017.He said the cup was about 15 degrees retroverted and slightly vertical.He also said he has never seen a head come out of a constrained liner without catastrophic failure, which this did not have, meaning liner became dislodged or screw and cup pull out.
Additional Manufacturer Narrative
The associated complaint device was not returned.A review of the manufacturing records did not reveal a manufacturing abnormality that could have caused or contributed to the reported incident.A review of complaint history on the listed part revealed no prior complaints for the listed batch with the same failure mode.A clinical analysis indicates that the femoral component dislocated out of the constrained liner when the patient was dressing.A single pre-op x-ray was provided, which confirms the reported dislocation.It was communicated that the existing femoral head was "relocated" into the existing r3 constrained liner; therefore there are no implants to return.No further clinical assessment is warranted.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: OXINIUM FEM HD 12/14 22 MM +8
• Common Device Name: PRSTHSIS, HIP, SEMCNSTRIND, MTALCRAMICPLYMR CMNTD R NN-POROUS, NCMNTD
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 1450 brooks road; memphis TN 38116
• MDR Report Key: 7077049
• Report Number: 1020279-2017-01182
• Device Sequence Number: 938963
• Product Code: LZO
• UDI-Device Identifier: 03596010488886
• UDI-Public: 03596010488886
• Combination Product (Y/N): N
• Initial Reporter State: AZ
• Initial Reporter Country: US
• PMA/510(K) Number: K021673
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 04/03/2018

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: Lay User/Patient
• Device Catalogue Number: 71342208
• Device Lot Number: 15EM19895
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 11/27/2017
• Supplement Date Received by Manufacturer: 11/27/2017
• Initial Report FDA Received Date: 12/01/2017
• Supplement Report FDA Received Date: 04/03/2018
• 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