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Recall for HemaCarotid Patch ultrathin knitted, InterVascular S.A.S.

2009.08.12

Product group Non-active implants
Reference 02542/09

InterVascular S.A.S. initiated a voluntary product recall of certain serial numbers of the HemaCarotid Patch ultrathin knitted due to mislabelling. There was no patient injury reported.

Recall for HemaCarotid Patch ultrathin knitted, InterVascular S.A.S. , Download_VeroeffentlichtAm_EN PDF, 73KB, File does not meet accessibility standards

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