Lot Recall for the product Modus 2.0 Cranial Plate, MEDARTIS
2013.09.17
Product group Non-active implants - bone surgery
Reference 04941/13
Modus 2.0 Cranial Plate: The company MEDARTIS has informed about a lot recall of devices. The action was initiated because of a labelling error in such a way that plates with a 0.7mm thickness were labeled as plates with 1mm thickness.
Lot Recall for the product Modus 2.0 Cranial Plate, MEDARTIS , Download_VeroeffentlichtAm_EN