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Recall for Ultrapro Mesh, Johnson & Johnson
2009.04.20
Product group Non-active implants
Reference 01017/09
Ultrapro Mesh: The company Johnson & Johnson has informed about a lot recall of this surgical mesh. The action was initiated because of an error in such a way that a lot intended for the US-market has been distributed to EU countries (in English language, without the CE-mark).
Recall for Ultrapro Mesh, Johnson & Johnson , Download_VeroeffentlichtAm_EN