The FDA recently designated a Medline Industries guidewires recall as Class I. The Medline guidewire is identified as the ACME Monaco Guidewire .035x150 3MMJ TCFC item number 88241, with affected products distributed between March 2013 and August 2013. The guidewire is used in various surgical convenience kits assembled and marketed by Medline Industries. It is meant to fit inside a percutaneous catheter for the purpose of directing the catheter through a blood vessel.
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