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2. No authors listed. United States Food and Drug Administration. Stryker initiates voluntary product recall of modular-neck stems: action specific to Rejuvenate and ABG II modular-neck stems. http://www.fda.gov/safety/recalls/ucm311043.htm (date last accessed 13 June 2013).
3. No authors listed. National Joint Registry for England and Wales: 9th annual report, 2012. http://www.njrcentre.org.uk (date last accessed 9 May 2013).
4. No authors listed. The National Joint Registry. Prostheses used in hip knee and ankle replacements, 2011. http://www.njrcentre.org.uk/njrcentre/Portals/0/Documents/England/Reports/9th_annual_report/Prostheses%20used%20in%20hip%20knee% 20and%20ankle%20replacements%202011.pdf (date last accessed 9 May 2013).