Which medical device recall in 2005-2006 led to the FDA implementing the Unique Device Identification (UDI) system for tracking medical devices throughout their lifecycle?

Product recalls in the medical industry can have life-or-death consequences and require sophisticated systems to track and notify healthcare providers. This poll tests your knowledge about one of the most significant medical device recalls in recent history, which transformed how the industry approaches product safety and tracking.

This is a live public trivia poll on AIPolls.Net. Vote and see real-time results.

Guidant's implantable cardioverter-defibrillators (ICDs) that short-circuited
DePuy's metal-on-metal hip implants that released metal debris
Baxter's Colleague infusion pumps with software and battery failures
Medtronic's Sprint Fidelis defibrillator leads that fractured prematurely