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Lot recall of devices for BioFoam Surgical Matrix, CRYOLIFE

2014.03.10

Product group Non-active implants - special implants
Reference 00812/14

BioFoam Surgical Matrix: The company CRYOLIFE has informed about a lot recall of devices. The action was initiated because of a labeling error in such a way that 5ml products were packaged in 2ml shelf boxes.

Lot recall of devices for BioFoam Surgical Matrix, CRYOLIFE , Download_VeroeffentlichtAm_EN PDF, 2MB, File does not meet accessibility standards

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