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