Recall of several batches of the product family Tissue-Guard (Vascu-Guard, Dura-Guard, Peri-Guard and Supple-Peri-Guard), Synovis/Baxter
2014.05.02
Product group Non-active implants - cardiac surgery
Reference 06421/13
The manufacturer Synovis/Baxter has conducted a recall of several batches of the product family Tissue-Guard (Vascu-Guard, Dura-Guard, Peri-Guard and Supple-Peri-Guard). Reason for the recall was the possibility of damaged packaging leading to leakage.
For further information as well as details concerning the device please see the enclosed Advisory Notice of the manufacturer.