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Safety Notice/Recall for the Bard Lifestent Vascular Stent System, Angiomed

Product group Non-active implants
Reference 00019/11

The manufacturer Angiomed GmbH performs a recall of 4 catalogue numbers (see Field Safety Notice) of the Bard Lifestent Vascular Stent System due to potential stent deployment failures.

Safety Notice/Recall for the Bard Lifestent Vascular Stent System, Angiomed , Download_VeroeffentlichtAm_EN PDF, 471KB, File does not meet accessibility standards