• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SMITH & NEPHEW ORTHOPAEDICS LTD. BHR; ACETABULAR CUP

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

SMITH & NEPHEW ORTHOPAEDICS LTD. BHR; ACETABULAR CUP Back to Search Results
Device Problems Device Operates Differently Than Expected (2913); Material Integrity Problem (2978)
Patient Problems Pain (1994); Swelling (2091); Weakness (2145); Chemical Exposure (2570); Test Result (2695)
Event Date 05/29/2013
Event Type  Injury  
Event Description
It was reported that revision surgery was performed due to pain, weakness of the legs and hips, elevated cobalt and chromium levels, and fluid accumulations around the hip.
 
Manufacturer Narrative
These combination of devices constitutes an off label application in the united states.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
BHR
Type of Device
ACETABULAR CUP
Manufacturer (Section D)
SMITH & NEPHEW ORTHOPAEDICS LTD.
1 kingmaker court
warwick technology park
warwick CV34 6WG
UK  CV34 6WG
Manufacturer (Section G)
SMITH & NEPHEW ORTHOPAEDICS, LTD.
1 kingmaker court
warwick technology park
warwick CV34 6WG
UK   CV34 6WG
Manufacturer Contact
michael simmonds
4419264823
MDR Report Key3567184
MDR Text Key4063190
Report Number3005477969-2014-00023
Device Sequence Number1
Product Code NXT
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
P040033
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer,Company Representative
Reporter Occupation Other
Type of Report Initial
Report Date 01/10/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received01/10/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received01/08/2014
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Treatment
HEMI HEAD, PART AND LOT # UNKNOWN
Patient Outcome(s) Hospitalization; Required Intervention;
-
-