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Updated Safety Notice / Recall for the ABGII Modular Systems, Stryker

Product group Non-active implants - bone surgery
Reference 03016/12

The manufacturer Stryker recalls the ABGII Modular Systems due to the potential for fretting and/or corrosion at or about the modular neck junctions. The recent FSCA extends the FSN dated April and May 2012 (please refer to the BfArM notice dated 08.06.2012 on this case).

Updated Safety Notice / Recall for the ABGII Modular Systems, Stryker , Download_VeroeffentlichtAm_EN PDF, 33KB, File does not meet accessibility standards