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Medtronic Recalls Dual Chamber IPGs

The FDA announced that on Jan 17, Medtronic, Inc. has issued a recall for Dual Chamber Implantable Pulse Generators (IPGs) due to a possible circuit error. This has been identified as a Class I recall – the most serious type of recall. Use of these devices may...
Announcing the NEW BidMed Exchange

Announcing the NEW BidMed Exchange

Reaching Buyers is Easier Than Ever! Our All-New Marketplace: the BidMed Exchange With a total refresh to our technology suite, sellers now have access to even more facilities on a platform designed specifically for the medical marketplace. And with integrated...