02
January
Important recall notice document

Following receipt of a recall notice from the manufacturer Teleflex Medical, we would like to inform our customers about the need to stop the sale of the devices code and batch listed in the recall notice document (here).
Therefore, if you have purchased such devices in the listed codes and batches, we ask that you do not use the product, isolate it, and appropriately identify it as NON-CONFORMING to avoid any kind of risk due to its use.
We will be sure to contact you again if we have more precise information and instructions on how to proceed from the manufacturer.

 


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