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Lot Recall of a TEP inlay, Stryker

2012.08.28

Product group Non-active implants - bone surgery
Reference 05992/11

The manufacturer Stryker recalls several lots of a TEP inlay. The CE labelling ended in 2007, nevertheless the device was distributed until April 2011.

Lot Recall of a TEP inlay, Stryker , Download_VeroeffentlichtAm_EN PDF, 30KB, File does not meet accessibility standards

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