Which medical device recall resulted in the FDA establishing the Unique Device Identification (UDI) system for improved traceability and patient safety?

Product recalls in the medical industry can have life-altering consequences and often reveal critical gaps in safety protocols. This trivia tests your knowledge about one of the most significant medical device recalls in recent history that changed industry standards. Understanding past failures helps medical professionals and product developers create safer healthcare solutions in the future.

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DePuy ASR hip implants (2010) - recalled after evidence showed a 12-13% failure rate requiring revision surgery within 5 years
Guidant defibrillators (2005) - recalled after reports of short-circuiting that led to at least 7 deaths
Bayer's Essure birth control device (2018) - pulled from market after thousands of women reported severe complications
Philips Respironics ventilators (2021) - recalled due to foam degradation that could release harmful particles into the airway