Which medical device recall in the 2000s led to the FDA establishing the Unique Device Identification (UDI) system to improve product tracking and patient safety?

In the high-stakes world of medicine, product recalls can significantly impact patient safety and healthcare delivery. This trivia question explores a notable medical product recall that changed industry practices. Test your knowledge of how regulatory bodies and manufacturers respond when medical products pose unexpected risks to patients. Understanding these historical cases helps healthcare professionals make informed decisions about the products they use in patient care.

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Guidant cardiac defibrillators (2005-2006)
DePuy ASR hip implants (2010)
Baxter Colleague infusion pumps (2010)
Bard IVC filters (2015)