Which medical device recall led to the FDA's establishment of the Unique Device Identification (UDI) system that revolutionized medical product tracking?

In the medical industry, product recalls can have life-or-death consequences. The process of identifying, communicating, and managing these recalls requires sophisticated systems and protocols that must balance patient safety, regulatory compliance, and business continuity. Test your knowledge about one of the most significant medical device recalls in recent history and its impact on the industry's approach to product safety monitoring.

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Guidant's implantable cardioverter-defibrillators recall (2005-2006)
Allergan's textured breast implant recall (2019)
Philips Respironics ventilator recall (2021)
DePuy's ASR hip implant recall (2010)